Nanotechnological Advances for Nose to Brain Delivery of Therapeutics to Improve the Parkinson Therapy
Open accessAbstract
Blood-Brain Barrier (BBB) acts as a highly impermeable barrier, presenting an impediment to the crossing of most classical drugs targeted for neurodegenerative diseases including Parkinson's disease (PD). About the nature of drugs and other potential molecules, they impose unavoidable doserestricted limitations eventually leading to the failure of therapy. However, many advancements in formulation technology and modification of delivery approaches have been successful in delivering the drug to the brain in the therapeutic window. The nose to the brain (N2B) drug delivery employing the nanoformulation, is one such emerging delivery approach, overcoming both classical drug formulation and delivery-associated limitations. This latter approach offers increased bioavailability, greater patient acceptance, lesser metabolic degradation of drugs, circumvention of BBB, ample drug loading along with the controlled release of the drugs. In N2B delivery, the intranasal (IN) route carries therapeutics firstly into the nasal cavity followed by the brain through olfactory and trigeminal nerve connections linked with nasal mucosa. The N2B delivery approach is being explored for delivering other biologicals like neuropeptides and mitochondria. Meanwhile, this N2B delivery system is associated with critical challenges consisting of mucociliary clearance, degradation by enzymes, and drug translocations by efflux mechanisms. These challenges finally culminated in the development of suitable surfacemodified nano-carriers and Focused- Ultrasound-Assisted IN as FUS-IN technique which has expanded the horizons of N2B drug delivery. Hence, nanotechnology, in collaboration with advances in the IN route of drug administration, has a diversified approach for treating PD. The present review discusses the physiology and limitation of IN delivery along with current advances in nanocarrier and technical development assisting N2B drug delivery.
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Limitations of intranasal administration include differences in nasal cavity shape, exact dosing, mucociliary elimination, drainage to the pharynx or lower part, and health status such as allergies or colds.
“However, there are also some limitations, including the difference in the shape of respective nasal cavities, the exact dosing of intranasal drugs, the mucociliary elimination, and the drainage to the pharynx or to the lower part.165 Moreover, the health status of the body also needs to think, otherwise, maybe someone occurs conditions such as allergies or colds, which is not suited for intranasal”
From The blood–brain barrier: Structure, regulation and drug delivery (2023) · cites this paper as [165]
The sections on challenges in nose-to-brain delivery and factors affecting nasal delivery describe mucociliary drug removal, dose-volume limits, drainage out of the nasal cavity, and impaired delivery during rhinitis or a common cold. The intranasal screening section also notes variation in nasal anatomy. The copy does not establish difficulty with exact dosing or specify drainage to the pharynx or lower regions; page numbers were not available. (LLM, conf=0.84)
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Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., Benveniste, H., Vates, G. E., Deane, R., Goldman, S. A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003748 · Cited by 5,824 · see citing works
A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules
Aspelund, A., Antila, S., Proulx, S. T., Karlsen, T. V., Karaman, S., Detmar, M., Wiig, H., & Alitalo, K. (2015) · Journal of Experimental Medicine · doi:10.1084/jem.20142290 · Cited by 2,198 · see citing works
Nasal mucociliary clearance as a factor in nasal drug delivery
Marttin, E., Schipper, N. G. M., Verhoef, J. C., & Merkus, F. W. H. M. (1998) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(97)00059-8 · Cited by 469 · see citing works
Hajak, G., Müller, W. E., Wittchen, H. U., Pittrow, D., & Kirch, W. (2003) · Addiction · doi:10.1046/j.1360-0443.2003.00491.x · Cited by 404 · see citing works
Recent advances in carrier mediated nose-to-brain delivery of pharmaceutics
Bourganis, V., Kammona, O., Alexopoulos, A., & Kiparissides, C. (2018) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2018.05.009 · Cited by 357 · see citing works
Pangeni, R., Sharma, S., Mustafa, G., Ali, J., & Baboota, S. (2014) · Nanotechnology · doi:10.1088/0957-4484/25/48/485102 · Cited by 192 · see citing works
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Research works printed but not linked: 153
- [1]Simon D.K. Tanner C.M. Brundin P. Parkinson disease epidemiology, pathology, genetics, and pathophysiology. Clin. Geriatr. Med. 2020 36 1 1 12 10.1016/j.cger.2019.08.002 31733690 PMC6905381 · DOI · Paper page
- [2]Maiti P. Manna J. Dunbar G.L. Maiti P. Dunbar G.L. Current understanding of the molecular mechanisms in Parkinson’s disease: Targets for potential treatments. Transl. Neurodegener. 2017 6 1 28 10.1186/s40035-017-0099-z 29090092 PMC5655877 · DOI
- [3]Gabathuler R. Approaches to transport therapeutic drugs across the blood-brain barrier to treat brain diseases. Neurobiol. Dis. 2010 37 1 48 57 10.1016/j.nbd.2009.07.028 19664710 · DOI
- [4]Kaur R. Mehan S. Singh S. Understanding multifactorial architecture of Parkinson’s disease: Pathophysiology to management. In: Neurological Sciences; Springer: Verlag Italia, 2019 40, pp. 13-23 30267336
- [5]Pajouhesh H. Lenz G.R. Medicinal chemical properties of successful central nervous system drugs. NeuroRx 2005 2 4 541 553 10.1602/neurorx.2.4.541 16489364 PMC1201314 · DOI
- [6]Engelhardt B. Sorokin L. The blood-brain and the blood-cerebrospinal fluid barriers: Function and dysfunction. Semin. Immunopathol. 2009 31 4 497 511 10.1007/s00281-009-0177-0 19779720 · DOI
- [7]Silindir G.M. Yekta O.A. Chalon S. Drug delivery systems for imaging and therapy of Parkinson’s disease. Curr. Neuropharmacol. 2016 14 4 376 391 10.2174/1570159X14666151230124904 26714584 PMC4876593 · DOI
- [8]Djupesland P.G. Messina J.C. Mahmoud R.A. The nasal approach to delivering treatment for brain diseases: An anatomic, physiologic, and delivery technology overview. Ther. Deliv. 2014 5 6 709 733 10.4155/tde.14.41 25090283 · DOI
- [9]Haddad F. Sawalha M. Khawaja Y. Najjar A. Karaman R. Dopamine and levodopa prodrugs for the treatment of Parkinson’s disease. Molecules 2017 23 1 40 10.3390/molecules23010040 29295587 PMC5943940 · DOI
- [10]Tambasco N. Romoli M. Calabresi P. Levodopa in Parkinson’s disease: Current status and future developments. Curr. Neuropharmacol. 2018 16 8 1239 1252 10.2174/1570159X15666170510143821 28494719 PMC6187751 · DOI
- [11]Joseph J. Motor fluctuations and dyskinesias in Parkinson’s disease: Clinical manifestations. Mov. Disord. 2005 20 Suppl. 11 S11 S16 15822109
- [12]Angela M.C. Presynaptic mechanisms of l-DOPA-induced dyskinesia: The findings, the debate, and the therapeutic implications. Front. Neurol. 2014 242 5 PMC4266027 25566170
- [13]Olarte-Avellaneda S. Cepeda Del Castillo J. Rojas-Rodriguez A.F. Sánchez O. Rodríguez-López A. Suárez G.D.A. Pulido L.M.S. Alméciga-Díaz C.J. Bromocriptine as a novel pharmacological chaperone for mucopolysaccharidosis IV A. ACS Med. Chem. Lett. 2020 11 7 1377 1385 10.1021/acsmedchemlett.0c00042 32676143 PMC7356376 · DOI
- [14]Brooks D.J. Dopamine agonists: Their role in the treatment of Parkinson’s disease. J. Neurol. Neurosurg. Psychiatry 2000 68 6 685 689 10.1136/jnnp.68.6.685 10811688 PMC1736955 · DOI
- [15]Olanow C.W. Kieburtz K. Leinonen M. Elmer L. Giladi N. Hauser R.A. Klepiskaya O.S. Kreitzman D.L. Lew M.F. Russell D.S. Kadosh S. Litman P. Friedman H. Linvah N. The PB Study Group, A randomized trial of a low-dose Rasagiline and Pramipexole combination (P2B001) in early Parkinson’s disease. Mov. Disord. 2017 32 5 783 789 10.1002/mds.26941 28370340 · DOI
- [16]Antonini A Abbruzzese G Barone P Bonuccelli U Lopiano L. Onofrj M. COMT inhibition with tolcapone in the treatment algorithm of patients with Parkinson’s disease (PD): Relevance for motor and non-motor features. Neuropsychiatr Dis Treat, 2008 4 1 A 1-9 PMC2515921 18728767
- [17]Onofrj M. Thomas A. Iacono D. Di Iorio A. Bonanni L. Switch-over from tolcapone to entacapone in severe Parkinson’s disease patients. Eur. Neurol. 2001 46 1 11 16 10.1159/000050749 11455177 · DOI
- [18]Parkinson Study Group Entacapone improves motor fluctuations in levodopa- treated Parkinson’s disease patients. Ann. Neurol. 1997 42 5 747 755 10.1002/ana.410420511 9392574 · DOI
- [19]Gordin A. Kaakkola S. Teräväinen H. Clinical advantages of COMT inhibition with entacapone - a review. J. Neural Transm. (Vienna) 2004 111 10-11 1343 1363 10.1007/s00702-004-0190-3 15340869 · DOI
- [20]Riederer P. Lachenmayer L. Laux G. Clinical applications of MAO-inhibitors. Curr. Med. Chem. 2004 11 15 2033 2043 10.2174/0929867043364775 15279566 · DOI
- [21]Schapira A.H. Monoamine oxidase B inhibitors for the treatment of Parkinson’s disease: A review of symptomatic and potential disease-modifying effects. CNS Drugs 2011 25 12 1061 1071 10.2165/11596310-000000000-00000 22133327 · DOI
- [22]Krishna R. Ali M. Moustafa A.A. Effects of combined MAO-B inhibitors and levodopa vs. monotherapy in Parkinson’s disease. Front. Aging Neurosci. 2014 6 JUL 180 25120478 PMC4111079
- [23]Schwab R.S. England A.C. Jr Poskanzer D.C. Young R.R. Amantadine in the treatment of Parkinson’s disease. JAMA 1969 208 7 1168 1170 10.1001/jama.1969.03160070046011 5818715 · DOI
- [24]Malkani R. Zadikoff C. Melen O. Videnovic A. Borushko E. Simuni T. Amantadine for freezing of gait in patients with Parkinson disease. Clin. Neuropharmacol. 2012 35 6 266 268 10.1097/WNF.0b013e31826e3406 23123688 PMC3690306 · DOI
- [25]Müller T. Drug therapy in patients with Parkinson’s disease. Transl. Neurodegener. 2012 1 1 10 10.1186/2047-9158-1-10 23211041 PMC3514092 · DOI
- [26]Current pharmacotherapy and screening models for Parkinson’s disease- a mini review. J. Nat. Remed., Available from: https://www.jnronline.com/ojs/index.php/about/article/view/192 [Accessed on: 2022 Jun, 1
- [27]Daniele A. Albanese A. Gainotti G. Gregori B. Bartolomeo P. Zolpidem in Parkinson’s disease. Lancet 1997 349 9060 1222 1223 10.1016/S0140-6736(05)62416-6 9130951 · DOI
- [29]Bronstein J.M. Tagliati M. Alterman R.L. Lozano A.M. Volkmann J. Stefani A. Horak F.B. Okun M.S. Foote K.D. Krack P. Pahwa R. Henderson J.M. Hariz M.I. Bakay R.A. Rezai A. Marks W.J. Jr Moro E. Vitek J.L. Weaver F.M. Gross R.E. DeLong M.R. Deep brain stimulation for Parkinson disease: An expert consensus and review of key issues. Arch. Neurol. 2011 68 2 165 171 10.1001/archneurol.2010.260 20937936 PMC4523130 · DOI
- [30]deSouza R.M. Moro E. Lang A.E. Schapira A.H.V. Timing of deep brain stimulation in Parkinson disease: A need for reappraisal? Ann. Neurol. 2013 73 5 565 575 10.1002/ana.23890 23483564 PMC4065356 · DOI
- [31]Deuschl G. Paschen S. Witt K. Clinical outcome of deep brain stimulation for Parkinson’s disease. Handb. Clin. Neurol. 2013 116 part II 107 128 10.1016/B978-0-444-53497-2.00010-3 24112889 · DOI
- [32]Tyulmankov D. Tass P.A. Bokil H. Periodic flashing coordinated reset stimulation paradigm reduces sensitivity to ON and OFF period durations. PLoS One 2018 13 9 e0203782 10.1371/journal.pone.0203782 30192855 PMC6128645 · DOI
- [33]Lenz F.A. Ablative surgery for the treatment of Parkinson’s disease. Handbook of Clinical Neurology. Elsevier 2007 243 260 18808951
- [34]Lang A.E. Obeso J.A. Challenges in Parkinson’s disease: Restoration of the nigrostriatal dopamine system is not enough. Lancet Neurol. 2004 3 5 309 316 10.1016/S1474-4422(04)00740-9 15099546 · DOI
- [35]Rivetti di Val Cervo P. Romanov R.A. Spigolon G. Masini D. Martín-Montañez E. Toledo E.M. Induction of functional dopamine neurons from human astrocytes in vitro and mouse astrocytes in a Parkinson’s disease model. Nat. Biotechnol. 2017 35 5 444 452 10.1038/nbt.3835 28398344 · DOI
- [36]Goodarzi P. Aghayan H.R. Larijani B. Soleimani M. Dehpour A.R. Sahebjam M. Ghaderi F. Arjmand B. Stem cell-based approach for the treatment of Parkinson’s disease. Med. J. Islam. Repub. Iran 2015 29 168 26000262 PMC4431356
- [38]Perez-Lloret S. Barrantes F.J. Deficits in cholinergic neurotransmission and their clinical correlates in Parkinson’s disease. NPJ Park. Dis. 2016 2 1 1 12 PMC5516588 28725692
- [39]Daniele A. Panza F. Greco A. Logroscino G. Seripa D. Can a positive allosteric modulation of GABAergic receptors improve motor symptoms in patients with Parkinson’s disease? The potential role of zolpidem in the treatment of Parkinson’s disease. Parkinsons Dis. 2016 2016 10.1155/2016/2531812 PMC4886078 27293955 · DOI
- [40]Lee D. Dallapiazza R. De Vloo P. Lozano A. Current surgical treatments for Parkinson’s disease and potential therapeutic targets. Neural Regen. Res. 2018 13 8 1342 1345 10.4103/1673-5374.235220 30106037 PMC6108190 · DOI
- [41]Md S. Bhattmisra S.K. Zeeshan F. Shahzad N. Mujtaba M.A. Srikanth Meka V. Radhakrishnan A. Kesharwani P. Baboota S. Ali J. Nano-carrier enabled drug delivery systems for nose to brain targeting for the treatment of neurodegenerative disorders. J. Drug Deliv. Sci. Technol. 2018 43 295 310 10.1016/j.jddst.2017.09.022 · DOI
- [42]Hussein N.R. Omer H.K. Elhissi A.M.A. Ahmed W. Advances in nasal drug delivery systems. In: Advances in Medical and Surgical Engineering. Elsevier Inc. 2020 279 311 10.1016/B978-0-12-819712-7.00015-2 · DOI
- [43]Hirlekar R.S. Momin A.M. Advances in drug delivery from nose to brain: An overview. Curr. Drug Ther. 2018 13 1 4 24 10.2174/1574885512666170921145204 · DOI
- [44]Selvaraj K. Gowthamarajan K. Karri V.V.S.R. Nose to brain transport pathways an overview: Potential of nanostructured lipid carriers in nose to brain targeting. Artif. Cells Nanomed. Biotechnol. 2018 46 8 2088 2095 29282995
- [47]Alexander A. Agrawal M. Bhupal Chougule M. Saraf S. Saraf S. Nose-to-brain drug delivery: An alternative approach for effective brain drug targeting. an alternative approach for effective brain drug targeting. In: Nanopharmaceuticals: Volume 1: Expectations and Realities of Multifunctional Drug Delivery Systems; Elsevier Inc. 2020 pp. 175-200
- [48]Ross T.M. Martinez P.M. Renner J.C. Thorne R.G. Hanson L.R. Frey W.H. II Intranasal administration of interferon beta bypasses the blood-brain barrier to target the central nervous system and cervical lymph nodes: A non-invasive treatment strategy for multiple sclerosis. J. Neuroimmunol. 2004 151 1-2 66 77 10.1016/j.jneuroim.2004.02.011 15145605 · DOI · Paper page
- [49]Thorne R.G. Pronk G.J. Padmanabhan V. Frey W.H. II Delivery of insulin-like growth factor-I to the rat brain and spinal cord along olfactory and trigeminal pathways following intranasal administration. Neuroscience 2004 127 2 481 496 10.1016/j.neuroscience.2004.05.029 15262337 · DOI · Paper page
- [50]Ghadiri M. Young P. Traini D. Strategies to enhance drug absorption via nasal and pulmonary routes. Pharmaceutics 2019 11 3 113 10.3390/pharmaceutics11030113 30861990 PMC6470976 · DOI
- [51]Keller L-A. Merkel O. Popp A. Intranasal drug delivery: Opportunities and toxicologic challenges during drug development. Drug Deliv. Transl. Res. 2021 2021 1 23 33491126 PMC7829061
- [54]Inoue D. Furubayashi T. Tanaka A. Sakane T. Sugano K. Effect of cerebrospinal fluid circulation on nose-to-brain direct delivery and distribution of caffeine in rats. Mol. Pharm. 2020 17 11 4067 4076 10.1021/acs.molpharmaceut.0c00495 32955898 · DOI
- [55]Lilius T.O. Blomqvist K. Hauglund N.L. Liu G. Stæger F.F. Bærentzen S. Du T. Ahlström F. Backman J.T. Kalso E.A. Rauhala P.V. Nedergaard M. Dexmedetomidine enhances glymphatic brain delivery of intrathecally administered drugs. J. Control. Release 2019 304 29 38 10.1016/j.jconrel.2019.05.005 31067483 · DOI
- [57]Anand U. Feridooni T. Agu R.U. Novel mucoadhesive polymers for nasal drug delivery. Recent Adv. Novel Drug Carrier Syst 2012 315 330 10.5772/52560 · DOI
- [58]Pathak R. Prasad Dash R. Misra M. Nivsarkar M. Role of mucoadhesive polymers in enhancing delivery of nimodipine microemulsion to brain via intranasal route. Acta Pharm. Sin. B 2014 4 2 151 160 10.1016/j.apsb.2014.02.002 26579378 PMC4590727 · DOI · Paper page
- [59]Chari S. Sridhar K. Walenga R. Kleinstreuer C. Computational analysis of a 3D mucociliary clearance model predicting nasal drug uptake. J. Aerosol Sci. 2021 155 105757 10.1016/j.jaerosci.2021.105757 · DOI
- [60]van Rumund A. Pavelka L. Esselink R.A.J. Geurtz B.P.M. Wevers R.A. Mollenhauer B. Peripheral decarboxylase inhibitors paradoxically induce aromatic L-amino acid decarboxylase. NPJ Park Dis 2021 7 1 1 5 PMC7979935 33741988
- [61]Cacciatore I. Ciulla M. Marinelli L. Eusepi P. Di Stefano A. Advances in prodrug design for Parkinson’s disease. Expert Opin. Drug Discov. 2018 13 4 295 305 10.1080/17460441.2018.1429400 29361853 · DOI
- [62]Bors L.A. Bajza Á. Mándoki M. Tasi B.J. Cserey G. Imre T. Szabó P. Erdő F. Modulation of nose-to-brain delivery of a P-glycoprotein (MDR1) substrate model drug (quinidine) in rats. Brain Res. Bull. 2020 160 65 73 10.1016/j.brainresbull.2020.04.012 32344126 · DOI
- [63]Dolberg A.M. Reichl S. Expression of P-glycoprotein in excised human nasal mucosa and optimized models of RPMI 2650 cells. Int. J. Pharm. 2016 508 1-2 22 33 10.1016/j.ijpharm.2016.05.010 27155589 · DOI
- [64]Di Gioia S. Trapani A. Mandracchia D. De Giglio E. Cometa S. Mangini V. Arnesano F. Belgiovine G. Castellani S. Pace L. Lavecchia M.A. Trapani G. Conese M. Puglisi G. Cassano T. Intranasal delivery of dopamine to the striatum using glycol chitosan/sulfobutylether-β-cyclodextrin based nanoparticles. Eur. J. Pharm. Biopharm. 2015 94 1 180 193 10.1016/j.ejpb.2015.05.019 26032293 · DOI
- [65]Nagpal K. Singh S.K. Mishra D.N. Chitosan nanoparticles: A promising system in novel drug delivery. Chem. Pharm. Bull. (Tokyo) 2010 58 11 1423 1430 10.1248/cpb.58.1423 21048331 · DOI
- [66]Henriksen I. Green K.L. Smart J.D. Smistad G. Karlsen J. Bioadhesion of hydrated chitosans: An in vitro and in vivo study. Int. J. Pharm. 1996 145 1-2 231 240 10.1016/S0378-5173(96)04776-X · DOI
- [67]Ozsoy Y. Gungor S. Cevher E. Nasal delivery of high molecular weight drugs. Molecules 2009 14 9 3754 3779 10.3390/molecules14093754 19783956 PMC6254717 · DOI
- [68]Raj R. Wairkar S. Sridhar V. Gaud R. Pramipexole dihydrochloride loaded chitosan nanoparticles for nose to brain delivery: Development, characterization and in vivo anti-Parkinson activity. Int. J. Biol. Macromol. 2018 109 27 35 10.1016/j.ijbiomac.2017.12.056 29247729 · DOI
- [69]Nguyen T.T. Dung Nguyen T.T. Vo T.K. Tran N.M.A. Nguyen M.K. Van Vo T. Van Vo G. Nanotechnology-based drug delivery for central nervous system disorders. Biomed. Pharmacother. 2021 143 112117 10.1016/j.biopha.2021.112117 34479020 · DOI
- [70]Mustafa G. Baboota S. Ahuja A. Ali J. Formulation development of chitosan coated intra nasal ropinirole nanoemulsion for better management option of parkinson: An in vitro ex vivo evaluation. Curr. Nanosci. 2012 8 3 348 360 10.2174/157341312800620331 · DOI
- [71]Bi C. Wang A. Chu Y. Liu S. Mu H. Liu W. Wu Z. Sun K. Li Y. Intranasal delivery of rotigotine to the brain with lactoferrin-modified PEG-PLGA nanoparticles for Parkinson’s disease treatment. Int. J. Nanomedicine 2016 11 6547 6559 10.2147/IJN.S120939 27994458 PMC5153272 · DOI
- [72]Sridhar V. Gaud, R.; Bajaj, A.; Wairkar, S. Pharmacokinetics and pharmacodynamics of intranasally administered selegiline nanoparticles with improved brain delivery in Parkinson’s disease. Nanomedicine (Lond.) 2018 14 8 2609 2618 30171904
- [73]Ahmad N. Rasagiline-encapsulated chitosan-coated PLGA nanoparticles targeted to the brain in the treatment of parkinson’s disease. 2017 40 13 677-690 10.1080/10826076.2017.1343735 · DOI
- [74]Choudhury H. Zakaria N.F.B. Tilang P.A.B. Tzeyung A.S. Pandey M. Chatterjee B. Alhakamy N.A. Bhattamishra S.K. Kesharwani P. Gorain B. Md S. Formulation development and evaluation of rotigotine mucoadhesive nanoemulsion for intranasal delivery. J. Drug Deliv. Sci. Technol. 2019 54 101301 10.1016/j.jddst.2019.101301 · DOI
- [75]Gaba B. Khan T. Haider M.F. Alam T. Baboota S. Parvez S. Ali J. Vitamin E loaded naringenin nanoemulsion via intranasal delivery for the management of oxidative stress in a 6-OHDA Parkinson’s disease model. BioMed Res. Int. 2019 2019 2382563 31111044 PMC6487130
- [77]Hernando S. Herran E. Figueiro-Silva J. Pedraz J.L. Igartua M. Carro E. Hernandez R.M. Intranasal administration of TAT-conjugated lipid nanocarriers loading GDNF for Parkinson’s disease. Mol. Neurobiol. 2018 55 1 145 155 10.1007/s12035-017-0728-7 28866799 · DOI
- [79]Kumar S. Dang S. Nigam K. Ali J. Baboota S. Selegiline nanoformulation in attenuation of oxidative stress and upregulation of dopamine in the brain for the treatment of Parkinson’s disease. Rejuvenation Res. 2018 21 5 464 476 10.1089/rej.2017.2035 29717617 · DOI
- [80]Jafarieh O. Md S. Ali M. Baboota S. Sahni J.K. Kumari B. Bhatnagar A. Ali J. Design, characterization, and evaluation of intranasal delivery of ropinirole-loaded mucoadhesive nanoparticles for brain targeting. Drug Dev. Ind. Pharm. 2015 41 10 1674 1681 10.3109/03639045.2014.991400 25496439 · DOI
- [81]Wang F. Yang Z. Liu M. Tao Y. Li Z. Wu Z. Gui S. Facile nose-to-brain delivery of rotigotine-loaded polymer micelles thermosensitive hydrogels: In vitro characterization and in vivo behavior study. Int. J. Pharm. 2020 577 119046 10.1016/j.ijpharm.2020.119046 31982559 · DOI
- [82]Ahmad E. Lv Y. Zhu Q. Qi J. Dong X. Zhao W. Chen Z. Wu W. Lu Y. TAT modification facilitates nose-to-brain transport of intact mPEG-PDLLA micelles: Evidence from aggregation-caused quenching probes. Appl. Mater. Today 2020 19 100556 10.1016/j.apmt.2020.100556 · DOI
- [83]Migliore M.M. Ortiz R. Dye S. Campbell R.B. Amiji M.M. Waszczak B.L. Neurotrophic and neuroprotective efficacy of intranasal GDNF in a rat model of Parkinson’s disease. Neuroscience 2014 274 11 23 10.1016/j.neuroscience.2014.05.019 24845869 · DOI
- [84]Pardeshi C.V. Rajput P.V. Belgamwar V.S. Tekade A.R. Surana S.J. Novel surface modified solid lipid nanoparticles as intranasal carriers for ropinirole hydrochloride: Application of factorial design approach. Drug Deliv. 2013 20 1 47 56 10.3109/10717544.2012.752421 23311653 · DOI · Paper page
- [85]Kumar M. Pandey R.S. Patra K.C. Jain S.K. Soni M.L. Dangi J.S. Madan J. Evaluation of neuropeptide loaded trimethyl chitosan nanoparticles for nose to brain delivery. Int. J. Biol. Macromol. 2013 61 189 195 10.1016/j.ijbiomac.2013.06.041 23831532 · DOI
- [86]Tan J.P.K. Voo Z.X. Lim S. Venkataraman S. Ng K.M. Gao S. Hedrick J.L. Yang Y.Y. Effective encapsulation of apomorphine into biodegradable polymeric nanoparticles through a reversible chemical bond for delivery across the blood-brain barrier. Nanomedicine 2019 17 236 245 10.1016/j.nano.2019.01.014 30738234 · DOI
- [87]Liao W. Liu Z. Zhang T. Sun S. ye, J.; Li, Z.; Mao, L.; Ren, J. Enhancement of anti-inflammatory properties of nobiletin in macrophages by a nano-emulsion preparation. J. Agric. Food Chem. 2018 66 1 91 98 10.1021/acs.jafc.7b03953 29236498 · DOI
- [88]Solans C. Izquierdo P. Nolla J. Azemar N. Garcia-Celma M.J. Nano-emulsions. Curr. Opin. Colloid Interface Sci. 2005 10 3-4 102 110 10.1016/j.cocis.2005.06.004 · DOI
- [89]Ashhar M.U. Kumar S. Ali J. Baboota S. CCRD based development of bromocriptine and glutathione nanoemulsion tailored ultrasonically for the combined anti-parkinson effect. Chem. Phys. Lipids 2021 235 105035 10.1016/j.chemphyslip.2020.105035 33400967 · DOI
- [90]Nehal N. Nabi B. Rehman S. Pathak A. Iqubal A. Khan S.A. Yar M.S. Parvez S. Baboota S. Ali J. Chitosan coated synergistically engineered nanoemulsion of Ropinirole and nigella oil in the management of Parkinson’s disease: Formulation perspective and in vitro and in vivo assessment. Int. J. Biol. Macromol. 2021 167 605 619 10.1016/j.ijbiomac.2020.11.207 33278450 · DOI
- [91]Hernando S. Gartziandia O. Herran E. Pedraz J.L. Igartua M. Hernandez R.M. Advances in nanomedicine for the treatment of Alzheimer’s and Parkinson’s diseases. Nanomedicine (Lond.) 2016 11 10 1267 1285 10.2217/nnm-2016-0019 27077453 · DOI
- [92]Sun Y. Li L. Xie H. Wang Y. Gao S. Zhang L. Bo F. Yang S. Feng A. Primary studies on construction and evaluation of ion-sensitive in situ gel loaded with paeonol-solid lipid nanoparticles for intranasal drug delivery. Int. J. Nanomedicine 2020 15 3137 3160 10.2147/IJN.S247935 32440115 PMC7210040 · DOI
- [93]Scherließ R. Nasal formulations for drug administration and characterization of nasal preparations in drug delivery. Ther. Deliv. 2020 11 3 183 191 10.4155/tde-2019-0086 32046624 · DOI
- [94]Shah B.M. Misra M. Shishoo C.J. Padh H. Nose to brain microemulsion-based drug delivery system of rivastigmine: Formulation and ex-vivo characterization. Drug Deliv. 2015 22 7 918 930 10.3109/10717544.2013.878857 24467601 PMC11133781 · DOI
- [95]Soares S. Sousa J. Pais A. Vitorino C. Nanomedicine: Principles, properties, and regulatory issues. Front Chem. 2018 6 360 10.3389/fchem.2018.00360 30177965 PMC6109690 · DOI
- [96]Bahadur S. Pardhi D.M. Rautio J. Rosenholm J.M. Pathak K. Intranasal nanoemulsions for direct nose-to-brain delivery of actives for cns disorders. Pharmaceutics 2020 12 12 1230 10.3390/pharmaceutics12121230 33352959 PMC7767046 · DOI
- [97]Choi J-Y. Park C.H. Lee J. Effect of polymer molecular weight on nanocomminution of poorly soluble drug. Drug Deliv. 2008 15 5 347 353 10.1080/10717540802039113 18763166 · DOI
- [98]Agrahari V. Burnouf P-A. Burnouf T. Agrahari V. Nanoformulation properties, characterization, and behavior in complex biological matrices: Challenges and opportunities for brain-targeted drug delivery applications and enhanced translational potential. Adv. Drug Deliv. Rev. 2019 148 146 180 30797956
- [100]Donovan M.D. Huang Y. Large molecule and particulate uptake in the nasal cavity: The effect of size on nasal absorption. Adv. Drug Deliv. Rev. 1998 29 1-2 147 155 10.1016/S0169-409X(97)00066-5 10837585 · DOI
- [101]Farzal Z. Basu S. Burke A. Fasanmade O.O. Lopez E.M. Bennett W.D. Ebert C.S. Jr Zanation A.M. Senior B.A. Kimbell J.S. Comparative study of simulated nebulized and spray particle deposition in chronic rhinosinusitis patients. Int. Forum Allergy Rhinol. 2019 9 7 746 758 10.1002/alr.22324 30821929 PMC7457377 · DOI
- [102]Kaur P. Garg T. Rath G. Goyal A.K. In situ nasal gel drug delivery: A novel approach for brain targeting through the mucosal membrane. Artif. Cells Nanomed. Biotechnol. 2016 44 4 1167 1176 25749276
- [103]Chand P. Pratibha; Gnanarajan, G.; Kothiyal, P. In situ gel: A review. Indian J. Pharm. Biol. Res. 2016 4 2 11 19 [IJPBR 10.30750/ijpbr.4.2.2 · DOI
- [105]Mujawar N. Ghatage S. Navale S. Sankpal B. Patil S. Patil S. Nasal drug delivery: Problem solution and its application. J. Curr. Pharma Res. 2014 4 3 1231 1245 10.33786/JCPR.2014.v04i03.008 · DOI
- [106]Pendolino A.L. Lund V.J. Nardello E. Ottaviano G. The nasal cycle: A comprehensive review. Rhinol. Online 2018 1 1 67 76 10.4193/RHINOL/18.021 · DOI
- [107]Schipper N.G.M. Verhoef J.C. Merkus F.W.H.M. The nasal mucociliary clearance: Relevance to nasal drug delivery. Pharm. Res. 1991 8 7 807 814 10.1023/A:1015830907632 1924131 · DOI
- [108]Trenkel M. Scherließ R. Nasal powder formulations: In-vitro characterisation of the impact of powders on nasal residence time and sensory effects. Pharm 2021 13 3 385 PMC8001606 33805779
- [109]Sharma S. Lohan S. Murthy R.S.R. Formulation and characterization of intranasal mucoadhesive nanoparticulates and thermo-reversible gel of levodopa for brain delivery. Drug Dev. Ind. Pharm. 2014 40 7 869 878 10.3109/03639045.2013.789051 23600649 · DOI
- [110]Inoue D. Furubayashi T. Tanaka A. Sakane T. Sugano K. Quantitative estimation of drug permeation through nasal mucosa using in vitro membrane permeability across Calu-3 cell layers for predicting in vivo bioavailability after intranasal administration to rats. Eur. J. Pharm. Biopharm. 2020 149 145 153 10.1016/j.ejpb.2020.02.004 32057906 · DOI
- [111]Kürti L. Veszelka S. Bocsik A. Ózsvári B. Puskás L.G. Kittel Á. Szabó-Révész P. Deli M.A. Retinoic acid and hydrocortisone strengthen the barrier function of human RPMI 2650 cells, a model for nasal epithelial permeability. Cytotechnology 2013 65 3 395 406 10.1007/s10616-012-9493-7 22940916 PMC3597180 · DOI
- [112]Zada M.H. Kubek M. Khan W. Kumar A. Domb A. Dispersible hydrolytically sensitive nanoparticles for nasal delivery of thyrotropin releasing hormone (TRH). J. Control. Release 2019 295 278 289 10.1016/j.jconrel.2018.12.050 30610951 · DOI
- [113]Mistry A. Stolnik S. Illum L. Nose-to-brain delivery: Investigation of the transport of nanoparticles with different surface characteristics and sizes in excised porcine olfactory epithelium. Mol. Pharm. 2015 12 8 2755 2766 10.1021/acs.molpharmaceut.5b00088 25997083 · DOI
- [114]Ladel S. Schlossbauer P. Flamm J. Luksch H. Mizaikoff B. Schindowski K. Improved in vitro model for intranasal mucosal drug delivery: Primary olfactory and respiratory epithelial cells compared with the permanent nasal cell line RPMI 2650. Pharm 2019 11 8 367 PMC6723747 31374872
- [115]Na K. Lee M. Shin H.W. Chung S. In vitro nasal mucosa gland-like structure formation on a chip. Lab Chip 2017 17 9 1578 1584 10.1039/C6LC01564F 28379223 · DOI
- [116]Nižić Nodilo L. Ugrina I. Špoljarić D. Amidžić Klarić D. Jakobušić Brala C. Perkušić M. Pepić I. Lovrić J. Saršon V. Safundžić Kučuk M. Zadravec D. Kalogjera L. Hafner A. A dry powder platform for nose-to-brain delivery of dexamethasone: Formulation development and nasal deposition studies. Pharmaceutics 2021 13 6 795 10.3390/pharmaceutics13060795 34073500 PMC8229415 · DOI
- [117]Trenfield SJ Awad A Madla CM Hatton GB Firth J Goyanes A Shaping the future: Recent advances of 3D printing in drug delivery and healthcare. 2019 16 10 1081-1094 31478752
- [118]Lungare S. Bowen J. Badhan R. Development and evaluation of a novel intranasal spray for the delivery of amantadine. J. Pharm. Sci. 2016 105 3 1209 1220 10.1016/j.xphs.2015.12.016 26886345 · DOI
- [119]Ahmad J. Haider N. Khan M.A. Md S. Alhakamy N.A. Ghoneim M.M. Alshehri S. Sarim Imam S. Ahmad M.Z. Mishra A. Novel therapeutic interventions for combating Parkinson’s disease and prospects of Nose-to-Brain drug delivery. Biochem. Pharmacol. 2022 195 114849 10.1016/j.bcp.2021.114849 34808125 · DOI
- [120]Khan S. Patil K. Bobade N. Yeole P. Gaikwad R. Formulation of intranasal mucoadhesive temperature-mediated in situ gel containing ropinirole and evaluation of brain targeting efficiency in rats. J. Drug Target. 2010 18 3 223 234 10.3109/10611860903386938 20030503 · DOI
- [121]Rao M. Agrawal D.K. Shirsath C. Thermoreversible mucoadhesive in situ nasal gel for treatment of Parkinson’s disease. Drug Dev. Ind. Pharm. 2017 43 1 142 150 10.1080/03639045.2016.1225754 27533244 · DOI
- [122]Ravi P.R. Aditya N. Patil S. Cherian L. Nasal in-situ gels for delivery of rasagiline mesylate: Improvement in bioavailability and brain localization. Drug Deliv. 2015 22 7 903 910 10.3109/10717544.2013.860501 24286183 PMC11132615 · DOI
- [123]Djupesland P.G. Messina J.C. Mahmoud R.A. Role of nasal casts for in vitro evaluation of nasal drug delivery and quantitative evaluation of various nasal casts. In: Therapeutic Delivery. UK Newlands Press Ltd London 2020 485 495 10.4155/tde-2020-0054 32727298 · DOI
- [124]Samoliński B.K. Grzanka A. Gotlib T. Changes in nasal cavity dimensions in children and adults by gender and age. Laryngoscope 2007 117 8 1429 1433 10.1097/MLG.0b013e318064e837 17607151 · DOI
- [125]Warnken Z.N. Smyth H.D.C. Davis D.A. Weitman S. Kuhn J.G. Williams R.O. III Williams I. Personalized medicine in nasal delivery: The use of patient-specific administration parameters to improve nasal drug targeting using 3D-printed nasal replica casts. Mol. Pharm. 2018 15 4 1392 1402 10.1021/acs.molpharmaceut.7b00702 29485888 · DOI
- [126]Kundoor V. Dalby R.N. Assessment of nasal spray deposition pattern in a silicone human nose model using a color-based method. Pharm. Res. 2009 27 1 30 36 19902337
- [127]Kiaee M. Wachtel H. Noga M.L. Martin A.R. Finlay W.H. An idealized geometry that mimics average nasal spray deposition in adults: A computational study. Comput. Biol. Med. 2019 107 206 217 10.1016/j.compbiomed.2019.02.013 30851506 · DOI
- [128]Vachhani S. Kleinstreuer C. Comparison of micron- and nano-particle transport in the human nasal cavity with a focus on the olfactory region. Comput. Biol. Med. 2021 128 104103 10.1016/j.compbiomed.2020.104103 33220592 · DOI
- [129]Shah V. Sharma M. Pandya R. Parikh R.K. Bharatiya B. Shukla A. Tsai H.C. Quality by design approach for an in situ gelling microemulsion of Lorazepam via intranasal route. Mater. Sci. Eng. C 2017 75 1231 1241 10.1016/j.msec.2017.03.002 28415411 · DOI
- [130]Ladel S. Flamm J. Zadeh A.S. Filzwieser D. Walter J-C. Schlossbauer, P Allogenic Fc domain-facilitated uptake of IgG in nasal lamina propria: Friend or foe for intranasal CNS delivery? Pharm 2018 10 3 107 PMC6161100 30050027
- [131]Khafaji A.S. Al; Donovan, MD Endocytic uptake of solid lipid nanoparticles by the nasal mucosa. Pharm 2021 13 5 761 10.3390/pharmaceutics13050761 PMC8161025 34065558 · DOI
- [132]Kanazawa T. Fukuda M. Suzuki N. Suzuki T. Novel methods for intranasal administration under inhalation anesthesia to evaluate nose-to-brain drug delivery. J. Vis. Exp. 2018 2018 141 p.e58485 30507914
- [133]Tolosa E. Martí M.J. Valldeoriola F. Molinuevo J.L. History of levodopa and dopamine agonists in Parkinson’s disease treatment. Neurology 1998 50 Suppl. 6 S2 S10 10.1212/WNL.50.6_Suppl_6.S2 9633679 · DOI
- [134]Kao H.D. Traboulsi A. Itoh S. Dittert L. Hussain A. Enhancement of the systemic and CNS specific delivery of L-dopa by the nasal administration of its water soluble prodrugs. Pharm. Res. 2000 17 8 978 984 10.1023/A:1007583422634 11028945 · DOI
- [135]Samaridou E. Walgrave H. Salta E. Álvarez D.M. Castro-López V. Loza M. Alonso M.J. Nose-to-brain delivery of enveloped RNA - cell permeating peptide nanocomplexes for the treatment of neurodegenerative diseases. Biomaterials 2020 230 119657 10.1016/j.biomaterials.2019.119657 31837821 · DOI
- [136]Agrawal M. Saraf S. Saraf S. Dubey S.K. Puri A. Gupta U. Kesharwani P. Ravichandiran V. Kumar P. Naidu V.G.M. Murty U.S. Ajazuddin; Alexander, A. Stimuli-responsive in situ gelling system for nose-to-brain drug delivery. J. Control. Release 2020 327 235 265 10.1016/j.jconrel.2020.07.044 32739524 · DOI
- [137]Hoare T.R. Kohane D.S. Hydrogels in drug delivery: Progress and challenges. Polymer (Guildf.) 2008 49 8 1993 2007 10.1016/j.polymer.2008.01.027 · DOI
- [138]Sosnik A. Seremeta K. Polymeric hydrogels as technology platform for drug delivery applications. Gels 2017 3 3 25 10.3390/gels3030025 30920522 PMC6318675 · DOI
- [139]Aderibigbe B.A. In situ-based gels for nose to brain delivery for the treatment of neurological diseases. Pharmaceutics 2018 10 2 40 10.3390/pharmaceutics10020040 29601486 PMC6027251 · DOI
- [141]Hoban D.B. Newland B. Moloney T.C. Howard L. Pandit A. Dowd E. The reduction in immunogenicity of neurotrophin overexpressing stem cells after intra-striatal transplantation by encapsulation in an in situ gelling collagen hydrogel. Biomaterials 2013 34 37 9420 9429 10.1016/j.biomaterials.2013.08.073 24054846 · DOI
- [142]Khafagy E.S. Kamei N. Fujiwara Y. Okumura H. Yuasa T. Kato M. Arime K. Nonomura A. Ogino H. Hirano S. Sugano S. Takeda-Morishita M. Systemic and brain delivery of leptin via intranasal coadministration with cell-penetrating peptides and its therapeutic potential for obesity. J. Control. Release 2020 319 397 406 10.1016/j.jconrel.2020.01.016 31926192 · DOI
- [143]Aly A.E-E. Waszczak B.L. Intranasal gene delivery for treating Parkinsons disease: Overcoming the blood-brain barrier. Exp. Opin. Drug Deliv. Informa Healthcare 2015 12 1923 1941 26289676
- [144]Dhuria S.V. Hanson L.R. Frey W.H. II Intranasal delivery to the central nervous system: Mechanisms and experimental considerations. J. Pharm. Sci. 2010 99 4 1654 1673 10.1002/jps.21924 19877171 · DOI · Paper page
- [145]Malerba F. Paoletti F. Capsoni S. Cattaneo A. Intranasal delivery of therapeutic proteins for neurological diseases. Expert Opin. Drug Deliv. 2011 8 10 1277 1296 10.1517/17425247.2011.588204 21619468 · DOI
- [146]Lochhead J.J. Thorne R.G. Intranasal delivery of biologics to the central nervous system. Adv. Drug Deliv. Rev. 2012 64 7 614 628 10.1016/j.addr.2011.11.002 22119441 · DOI · Paper page
- [147]Lu C.T. Jin R.R. Jiang Y.N. Lin Q. Yu W.Z. Mao K.L. Tian F.R. Zhao Y.P. Zhao Y.Z. Gelatin nanoparticle-mediated intranasal delivery of substance P protects against 6-hydroxydopamine-induced apoptosis: An in vitro and in vivo study. Drug Des. Devel. Ther. 2015 9 1955 1962 25897205 PMC4396575
- [148]Samaridou E. Alonso M.J. María J.A. Epithelium O. Nose-to-brain peptide delivery-the potential of nanotechnology. Bioorg. Med. Chem. 2018 26 10 2888 2905 29170026
- [149]Decressac M. Pain S. Chabeauti P.Y. Frangeul L. Thiriet N. Herzog H. Vergote J. Chalon S. Jaber M. Gaillard A. Neuroprotection by neuropeptide Y in cell and animal models of Parkinson’s disease. Neurobiol. Aging 2012 33 9 2125 2137 10.1016/j.neurobiolaging.2011.06.018 21816512 · DOI
- [150]Duarte-Neves J. Cavadas C. Pereira de Almeida L. Neuropeptide Y. NPY) intranasal delivery alleviates Machado-Joseph disease. Sci. Reports 2021 11 1 1 9 PMC7870889 33558582
- [152]Mathé A.A. Michaneck M. Berg E. Charney D.S. Murrough J.W. A randomized controlled trial of intranasal neuropeptide Y in patients with major depressive disorder. Int. J. Neuropsychopharmacol. 2020 23 12 783 790 10.1093/ijnp/pyaa054 33009815 PMC7770516 · DOI
- [153]Noè F. Pool A.H. Nissinen J. Gobbi M. Bland R. Rizzi M. Balducci C. Ferraguti F. Sperk G. During M.J. Pitkänen A. Vezzani A. Neuropeptide Y gene therapy decreases chronic spontaneous seizures in a rat model of temporal lobe epilepsy. Brain 2008 131 6 1506 1515 10.1093/brain/awn079 18477594 · DOI
- [154]Fiebich B.L. Schleicher S. Butcher R.D. Craig A. Lieb K. The neuropeptide substance P activates p38 mitogen-activated protein kinase resulting in IL-6 expression independently from NF-κ. B. J. Immunol. 2000 165 10 5606 5611 10.4049/jimmunol.165.10.5606 11067916 · DOI
- [155]Zhao Y.Z. Jin R.R. Yang W. Xiang Q. Yu W.Z. Lin Q. Tian F.R. Mao K.L. Lv C.Z. Wáng Y.X.J. Lu C.T. Using gelatin nanoparticle mediated intranasal delivery of neuropeptide substance P to enhance neuro-recovery in hemiparkinsonian rats. PLoS One 2016 11 2 e0148848 10.1371/journal.pone.0148848 26894626 PMC4760767 · DOI
- [156]Rizk S.S. Misiura A. Paduch M. Kossiakoff A.A. Substance P derivatives as versatile tools for specific delivery of various types of biomolecular cargo. Bioconjug. Chem. 2012 23 1 42 46 10.1021/bc200496e 22175275 PMC3268364 · DOI
- [157]Ding G. Wang T. Han Z. Tian L. Cheng Q. Luo L. Zhao B. Wang C. Feng S. Wang L. Meng Z. Meng Q. Substance P containing peptide gene delivery vectors for specifically transfecting glioma cells mediated by a neurokinin-1 receptor. J. Mater. Chem. B Mater. Biol. Med. 2021 9 32 6347 6356 10.1039/D1TB00577D 34251002 · DOI
- [158]Bender T.S. Migliore M.M. Campbell R.B. John Gatley S. Waszczak B.L. Intranasal administration of glial-derived neurotrophic factor (GDNF) rapidly and significantly increases whole-brain GDNF level in rats. Neuroscience 2015 303 569 576 10.1016/j.neuroscience.2015.07.016 26166725 · DOI
- [159]Kordower J.H. Bjorklund A. Trophic factor gene therapy for Parkinson’s disease. Mov. Disord. 2013 28 1 96 109 10.1002/mds.25344 23390096 · DOI
- [160]Murlidharan G. Samulski R.J. Asokan A. Biology of adeno-associated viral vectors in the central nervous system. Front. Mol. Neurosci. 2014 7 76 10.3389/fnmol.2014.00076 25285067 PMC4168676 · DOI
- [161]Tenenbaum L. Chtarto A. Lehtonen E. Velu T. Brotchi J. Levivier M. Recombinant AAV-mediated gene delivery to the central nervous system. J. Gene Med. 2004 6 Suppl. 1 S212 S222 14978764
- [162]McCully J.D. Cowan D.B. Emani S.M. del Nido P.J. Mitochondrial transplantation: From animal models to clinical use in humans. Mitochondrion 2017 34 127 134 10.1016/j.mito.2017.03.004 28342934 · DOI
- [163]Chang J-C. Chao Y-C. Chang H-S. Wu Y-L. Chang H-J. Lin, Y-S Intranasal delivery of mitochondria for treatment of Parkinson’s Disease model rats lesioned with 6-hydroxydopamine. Sci. Reports 2021 11 1 1 14 PMC8136477 34011937
- [164]Alexander J.F. Seua A.V. Arroyo L.D. Ray P.R. Wangzhou A. Heiβ-Lückemann L. Schedlowski M. Price T.J. Kavelaars A. Heijnen C.J. Nasal administration of mitochondria reverses chemotherapy-induced cognitive deficits. Theranostics 2021 11 7 3109 3130 10.7150/thno.53474 33537077 PMC7847685 · DOI
- [165]Chen H. Yang G.Z.X. Getachew H. Acosta C. Sierra Sánchez C. Konofagou E.E. Focused ultrasound-enhanced intranasal brain delivery of brain-derived neurotrophic factor. Sci. Rep. 2016 6 1 28599 10.1038/srep28599 27345430 PMC4921840 · DOI
- [166]Ji R. Smith M. Niimi Y. Karakatsani M.E. Murillo M.F. Jackson-Lewis V. Przedborski S. Konofagou E.E. Focused ultrasound enhanced intranasal delivery of brain derived neurotrophic factor produces neurorestorative effects in a Parkinson’s disease mouse model. Sci. Rep. 2019 9 1 19402 10.1038/s41598-019-55294-5 31852909 PMC6920380 · DOI
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The blood–brain barrier: Structure, regulation and drug delivery
Wu, D., Chen, Q., Chen, X., Han, F., Chen, Z., & Wang, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01481-w · Cited by 1,906 · see citing works
“However, there are also some limitations, including the difference in the shape of respective nasal cavities, the exact dosing of intranasal drugs, the mucociliary elimination, and the drainage to the pharynx or to the lower part.(165) Moreover, the health status of the body also needs to think, otherwise, maybe someo…”
Background
- Authors
- Khatri, D. K., Preeti, K., Tonape, S., Bhattacharjee, S., Patel, M., Shah, S., Singh, P. K., Srivastava, S., Gugulothu, D., Vora, L., & Singh, S. B.
- Affiliations
- National Institute of Pharmaceutical Education and Research (IN)
- Delhi Pharmaceutical Science and Research University (IN)
- Queen's University Belfast (GB)
- Corresponding author
- Khatri, Dharmendra K.
- Singh, Shashi B.
- ORCID
- Venue
- Current Neuropharmacology
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2023-03
- Volume
- 21
- Issue
- 3
- Pages
- 493-516
- ISSN
- 1570-159X (ISSN-L)
- PMC
- PMC10207920
- OpenAlex
- W4229030668
- Cited by
- 75
- References
- 6
- Citations by year
- 2026: 15 · 2025: 25 · 2024: 20 · 2023: 12 · 2022: 3
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc
- Locations
- Current Neuropharmacology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Research Portal (Queen's University Belfast) (submittedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Inhalation and Respiratory Drug Delivery
- Keywords
- nose-to-brain delivery, Parkinson's disease, blood-brain barrier, intranasal drug delivery, nanocarriers, mucociliary clearance, drug efflux, mitochondrial delivery, controlled drug release
- MeSH terms
- Blood-Brain Barrier, Brain, Humans, Nasal Mucosa, Parkinson Disease, Drug Delivery Systems, Nanotechnology
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