The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Intranasal drug delivery: An efficient and non-invasive route for systemic administration
Abstract
Intranasal administration is a non-invasive route for drug delivery, which is widely used for the local treatment of rhinitis or nasal polyposis. Since drugs can be absorbed into the systemic circulation through the nasal mucosa, this route may also be used in a range of acute or chronic conditions requiring considerable systemic exposure. Indeed, it offers advantages such as ease of administration, rapid onset of action, and avoidance of first-pass metabolism, which consequently offers for example an interesting alternative to intravenous, subcutaneous, oral transmucosal, oral or rectal administration in the management of pain with opioids. Given these indisputable interests, fentanyl-containing formulations have been recently approved and marketed for the treatment of breakthrough cancer pain. This review will outline the relevant aspects of the therapeutic interest and limits of intranasal delivery of drugs, with a special focus on opioids, together with an in-depth discussion of the physiological characteristics of the nasal cavity as well as physicochemical properties (lipophilicity, molecular weight, ionisation) and pharmaceutical factors (absorption enhancers, devices for application) that should be considered for the development of nasal drugs.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“intranasal delivery of small molecules and peptides including insulin has been shown to increase their biological effect in the brain (Grassin-Delyle et al., 2012).”
From Reversal of ApoE4-induced recycling block as a novel prevention approach for Alzheimer’s disease (2018) · cites this paper as Grassin-Delyle et al., 2012
Citations
Cites
Intranasal Drug Delivery: How, Why and What For?
Pires, A., Fortuna, A., Alves, G., & Falcão, A. (2009) · Journal of Pharmacy & Pharmaceutical Sciences · doi:10.18433/j3nc79 · Cited by 641
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
The biopharmaceutical aspects of nasal mucoadhesive drug delivery
Ugwoke, M. I., Verbeke, N., & Kinget, R. (2001) · Journal of Pharmacy and Pharmacology · doi:10.1211/0022357011775145 · Cited by 355
Flagged first, then by citations
Research works printed but not linked: 163
- 2011, Abstral (fentanyl sublingual tablets for breakthrough cancer pain), P T, 36, 2
- Agu, 2011, Differential expression of organic cation transporters in normal and polyps human nasal epithelium: implications for in vitro drug delivery studies, Int J Pharm, 406, 49, 10.1016/j.ijpharm.2010.12.037 · DOI
- Akerlund, 1993, Effect of oxymetazoline on nasal and sinus mucosal blood flow in the rabbit as measured with laser-Doppler flowmetry, Ann Otol Rhinol Laryngol, 102, 123, 10.1177/000348949310200209 · DOI
- Al Suleimani, 2007, Allergic rhinitis and its pharmacology, Pharmacol Ther, 114, 233, 10.1016/j.pharmthera.2007.01.012 · DOI
- Amidi, 2010, Chitosan-based delivery systems for protein therapeutics and antigens, Adv Drug Deliv Rev, 62, 59, 10.1016/j.addr.2009.11.009 · DOI
- Arora, 2002, Permeability issues in nasal drug delivery, Drug Discov Today, 7, 967, 10.1016/S1359-6446(02)02452-2 · DOI
- Baker, 2003, The effect of nitric oxide on the permeability of nasal epithelial cells from healthy and asthmatic donors, Med Sci Monit, 9, BR276
- Barton, 2005, Efficacy of intranasal naloxone as a needleless alternative for treatment of opioid overdose in the prehospital setting, J Emerg Med, 29, 265, 10.1016/j.jemermed.2005.03.007 · DOI
- Behl, 1998, Effects of physicochemical properties and other factors on systemic nasal drug delivery, Adv Drug Deliv Rev, 29, 89, 10.1016/S0169-409X(97)00063-X · DOI
- Benninger, 2004, Techniques of intranasal steroid use, Otolaryngol Head Neck Surg, 130, 5, 10.1016/j.otohns.2003.10.007 · DOI
- Bernkop-Schnurch, 1998, The use of inhibitory agents to overcome the enzymatic barrier to perorally administered therapeutic peptides and proteins, J Control Release, 52, 1, 10.1016/S0168-3659(97)00204-6 · DOI
- Bonsmann, 2001, Presence of fluticasone propionate on human nasal mucosal surface and in human nasal tissue over a period of 24 h after intranasal application, Allergy, 56, 532, 10.1034/j.1398-9995.2001.056006532.x · DOI
- Borland, 2007, A randomized controlled trial comparing intranasal fentanyl to intravenous morphine for managing acute pain in children in the emergency department, Ann Emerg Med, 49, 335, 10.1016/j.annemergmed.2006.06.016 · DOI
- Borland, 2011, Equivalency of two concentrations of fentanyl administered by the intranasal route for acute analgesia in children in a paediatric emergency department: a randomized controlled trial, Emerg Med Australas, 23, 202, 10.1111/j.1742-6723.2011.01391.x · DOI
- Born, 2002, Sniffing neuropeptides: a transnasal approach to the human brain, Nat Neurosci, 5, 514, 10.1038/nn0602-849 · DOI · Paper page
- Bourget, 1995, Study of the bioequivalence of two controlled-release formulations of morphine, Int J Clin Pharmacol Ther, 33, 588
- Cass, 1999, Pharmacokinetics of zanamivir after intravenous, oral, inhaled or intranasal administration to healthy volunteers, Clin Pharmacokinet, 36, 1, 10.2165/00003088-199936001-00001 · DOI
- Charlton, 2007, Evaluation of bioadhesive polymers as delivery systems for nose to brain delivery: in vitro characterisation studies, J Control Release, 118, 225, 10.1016/j.jconrel.2006.12.014 · DOI
- Cheng, 2007, Computation of octanol–water partition coefficients by guiding an additive model with knowledge, J Chem Inf Model, 47, 2140, 10.1021/ci700257y · DOI
- Cho, 2010, Characterization and in vitro evaluation of freeze-dried microparticles composed of granisetron–cyclodextrin complex and carboxymethylcellulose for intranasal delivery, Int J Pharm, 400, 59, 10.1016/j.ijpharm.2010.08.030 · DOI
- Christrup, 2008, Pharmacokinetics, efficacy, and tolerability of fentanyl following intranasal versus intravenous administration in adults undergoing third-molar extraction: a randomized, double-blind, double-dummy, two-way, crossover study, Clin Ther, 30, 469, 10.1016/j.clinthera.2008.03.001 · DOI
- Coda, 2003, Pharmacokinetics and bioavailability of single-dose intranasal hydromorphone hydrochloride in healthy volunteers, Anesth Analg, 97, 117, 10.1213/01.ANE.0000066311.40978.4F · DOI
- Costantino, 2007, Intranasal delivery: physicochemical and therapeutic aspects, Int J Pharm, 337, 1, 10.1016/j.ijpharm.2007.03.025 · DOI
- Dale, 2002, Disposition of nasal, intravenous, and oral methadone in healthy volunteers, Clin Pharmacol Ther, 72, 536, 10.1067/mcp.2002.128386 · DOI
- Darwish, 2007, Absorption of fentanyl from fentanyl buccal tablet in cancer patients with or without oral mucositis: a pilot study, Clin Drug Investig, 27, 605, 10.2165/00044011-200727090-00002 · DOI
- Darwish, 2005, Pharmacokinetics and dose proportionality of fentanyl effervescent buccal tablets in healthy volunteers, Clin Pharmacokinet, 44, 1279, 10.2165/00003088-200544120-00006 · DOI
- Darwish, 2006, Clin Ther, 28, 715, 10.1016/j.clinthera.2006.05.016 · DOI
- Davis, 2003, Absorption enhancers for nasal drug delivery, Clin Pharmacokinet, 42, 1107, 10.2165/00003088-200342130-00003 · DOI
- Davis, 2004, Pharmacokinetics of butorphanol tartrate administered from single-dose intranasal sprayer, Am J Health Syst Pharm, 61, 261, 10.1093/ajhp/61.3.261 · DOI
- Davis, 2005, Bioavailability of intranasal butorphanol administered from a single-dose sprayer, Am J Health Syst Pharm, 62, 48, 10.1093/ajhp/62.1.48 · DOI
- Davis, 2004, Bioavailability and pharmacokinetics of intranasal hydromorphone in patients experiencing vasomotor rhinitis, Clin Drug Investig, 24, 633, 10.2165/00044011-200424110-00002 · DOI
- Davis, 2004, Effect of fluticasone propionate nasal spray on bioavailability of intranasal hydromorphone hydrochloride in patients with allergic rhinitis, Pharmacotherapy, 24, 26, 10.1592/phco.24.1.26.34810 · DOI
- Devillier, 1988, Nasal response to substance P and methacholine in subjects with and without allergic rhinitis, Eur Respir J, 1, 356, 10.1183/09031936.93.01040356 · DOI
- Dhuria, 2009, Novel vasoconstrictor formulation to enhance intranasal targeting of neuropeptide therapeutics to the central nervous system, J Pharmacol Exp Ther, 328, 312, 10.1124/jpet.108.145565 · DOI
- Ding, 2003, Human extrahepatic cytochromes P450: function in xenobiotic metabolism and tissue-selective chemical toxicity in the respiratory and gastrointestinal tracts, Annu Rev Pharmacol Toxicol, 43, 149, 10.1146/annurev.pharmtox.43.100901.140251 · DOI
- Dowley, 2001, The effect of inferior turbinate hypertrophy on nasal spray distribution to the middle meatus, Clin Otolaryngol Allied Sci, 26, 488, 10.1046/j.1365-2273.2001.00509.x · DOI
- Dowling, 2008, Population pharmacokinetics of intravenous, intramuscular, and intranasal naloxone in human volunteers, Ther Drug Monit, 30, 490, 10.1097/FTD.0b013e3181816214 · DOI
- Duan, 2010, New strategies to improve the intranasal absorption of insulin, Drug Discov Today, 15, 416, 10.1016/j.drudis.2010.03.011 · DOI
- Duquesnoy, 1998, Comparative clinical pharmacokinetics of single doses of sumatriptan following subcutaneous, oral, rectal and intranasal administration, Eur J Pharm Sci, 6, 99, 10.1016/S0928-0987(97)00073-0 · DOI
- Edman, 1992, Microspheres as a nasal delivery system for peptide drugs, J Control Release, 21, 165, 10.1016/0168-3659(92)90018-M · DOI
- Edwards, 2003, Hydromorphone transfer into breast milk after intranasal administration, Pharmacotherapy, 23, 153, 10.1592/phco.23.2.153.32081 · DOI
- Eriksen, 1989, The systemic availability of buprenorphine administered by nasal spray, J Pharm Pharmacol, 41, 803, 10.1111/j.2042-7158.1989.tb06374.x · DOI
- Fisher, 2010, Pharmacokinetic comparisons of three nasal fentanyl formulations; pectin, chitosan and chitosan–poloxamer 188, Int J Clin Pharmacol Ther, 48, 138, 10.5414/CPP48138 · DOI
- Fitzgibbon, 2003, Initial pharmacokinetic, safety and efficacy evaluation of nasal morphine gluconate for breakthrough pain in cancer patients, Pain, 106, 309, 10.1016/S0304-3959(03)00318-X · DOI
- Foo, 2007, The influence of spray properties on intranasal deposition, J Aerosol Med, 20, 495, 10.1089/jam.2007.0638 · DOI
- Foster, 2008, Pharmacokinetics and pharmacodynamics of intranasal versus intravenous fentanyl in patients with pain after oral surgery, Ann Pharmacother, 42, 1380, 10.1345/aph.1L168 · DOI
- Gourlay, 1997, Arteriovenous differences in plasma concentration of nicotine and catecholamines and related cardiovascular effects after smoking, nicotine nasal spray, and intravenous nicotine, Clin Pharmacol Ther, 62, 453, 10.1016/S0009-9236(97)90124-7 · DOI
- Graff, 2003, P-Glycoprotein attenuates brain uptake of substrates after nasal instillation, Pharm Res, 20, 1225, 10.1023/A:1025053115583 · DOI
- Graff, 2005, Nasal drug administration: potential for targeted central nervous system delivery, J Pharm Sci, 94, 1187, 10.1002/jps.20318 · DOI
- Grape, 2010, Formulations of fentanyl for the management of pain, Drugs, 70, 57, 10.2165/11531740-000000000-00000 · DOI
- Greiff, 1994, Human nasal absorption of 51Cr-EDTA in smokers and control subjects, Clin Exp Allergy, 24, 1036, 10.1111/j.1365-2222.1994.tb02740.x · DOI
- Guthrie, 1999, Arterial/venous plasma nicotine concentrations following nicotine nasal spray, Eur J Clin Pharmacol, 55, 639, 10.1007/s002280050686 · DOI
- Gyi, 1994, Effect of halothane on cilia beat frequency of ciliated human respiratory epithelium in vitro, Br J Anaesth, 73, 507, 10.1093/bja/73.4.507 · DOI
- Haschke, 2010, Pharmacokinetics and pharmacodynamics of nasally delivered midazolam, Br J Clin Pharmacol, 69, 607, 10.1111/j.1365-2125.2010.03611.x · DOI
- Haugen, 2010, Assessment and classification of cancer breakthrough pain: a systematic literature review, Pain, 149, 476, 10.1016/j.pain.2010.02.035 · DOI
- Helmers, 1989, Comparison of intravenous and intranasal sufentanil absorption and sedation, Can J Anaesth, 36, 494, 10.1007/BF03005373 · DOI
- Henriksson, 1997, Expression of P-glycoprotein 170 in nasal mucosa may be increased with topical steroids, Am J Rhinol, 11, 317, 10.2500/105065897781446603 · DOI
- Henthorn, 1999, Active transport of fentanyl by the blood–brain barrier, J Pharmacol Exp Ther, 289, 1084, 10.1016/S0022-3565(24)38239-4 · DOI
- Hermens, 1987, The in vitro effect of morphine, fentanyl and sufentanil in ciliary beat frequency of human nasal epithelial tissue, Acta Pharm Technol, 33, 88
- Homer, 1998, An endoscopic photographic comparison of nasal drug delivery by aqueous spray, Clin Otolaryngol Allied Sci, 23, 560, 10.1046/j.1365-2273.1998.2360560.x · DOI
- Hybbinette, 1982, Effects of sympathomimetic agonists and antagonists on mucociliary activity, Acta Otolaryngol, 94, 121, 10.3109/00016488209128896 · DOI
- Hybbinette, 1982, Effects of the parasympathomimetic drug methacholine and its antagonist atropine on mucociliary activity, Acta Otolaryngol, 93, 465, 10.3109/00016488209130906 · DOI
- Illum, 1996, Nasal delivery. The use of animal models to predict performance in man, J Drug Target, 3, 427, 10.3109/10611869609015963 · DOI
- Illum, 2000, Transport of drugs from the nasal cavity to the central nervous system, Eur J Pharm Sci, 11, 1, 10.1016/S0928-0987(00)00087-7 · DOI · Paper page
- Illum, 2003, Nasal drug delivery—possibilities, problems and solutions, J Control Release, 87, 187, 10.1016/S0168-3659(02)00363-2 · DOI
- Illum, 2004, Is nose-to-brain transport of drugs in man a reality?, J Pharm Pharmacol, 56, 3, 10.1211/0022357022539 · DOI
- Illum, 1994, Chitosan as a novel nasal delivery system for peptide drugs, Pharm Res, 11, 1186, 10.1023/A:1018901302450 · DOI
- Illum, 1987, Bioadhesive microspheres as a potential nasal drug delivery system, Int J Pharm, 39, 189, 10.1016/0378-5173(87)90216-X · DOI
- Illum, 2002, Intranasal delivery of morphine, J Pharmacol Exp Ther, 301, 391, 10.1124/jpet.301.1.391 · DOI
- Ingels, 1992, Influence of sympathetic and parasympathetic substances in clinical concentrations on human nasal ciliary beat, Rhinology, 30, 149
- Inui, 2000, Cellular and molecular aspects of drug transport in the kidney, Kidney Int, 58, 944, 10.1046/j.1523-1755.2000.00251.x · DOI
- Irie, 1992, Enhancing effects of cyclodextrins on nasal absorption of insulin in rats, Int J Pharm, 84, 129, 10.1016/0378-5173(92)90053-5 · DOI
- Ishikawa, 2002, Insoluble powder formulation as an effective nasal drug delivery system, Pharm Res, 19, 1097, 10.1023/A:1019881706159 · DOI
- Kaasa, 2010, Pharmacokinetics of intranasal fentanyl spray in patients with cancer and breakthrough pain, J Opioid Manag, 6, 17, 10.5055/jom.2010.0001 · DOI
- Kamel, 2004, Nasal and paranasal sinus changes after radiotherapy for nasopharyngeal carcinoma, Acta Otolaryngol, 124, 532, 10.1080/00016480410018106 · DOI
- Kanthakumar, 1994, Effect of salmeterol on human nasal epithelial cell ciliary beating: inhibition of the ciliotoxin, pyocyanin, Br J Pharmacol, 112, 493, 10.1111/j.1476-5381.1994.tb13100.x · DOI
- Karasulu, 2008, Permeation studies and histological examination of sheep nasal mucosa following administration of different nasal formulations with or without absorption enhancers, Drug Deliv, 15, 219, 10.1080/10717540802006377 · DOI
- Karl, 1992, Comparison of the safety and efficacy of intranasal midazolam or sufentanil for preinduction of anesthesia in pediatric patients, Anesthesiology, 76, 209, 10.1097/00000542-199202000-00009 · DOI
- Kato, 2008, Intestinal first-pass metabolism of CYP3A4 substrates, Drug Metab Pharmacokinet, 23, 87, 10.2133/dmpk.23.87 · DOI
- Koepsell, 1998, Organic cation transporters in intestine, kidney, liver, and brain, Annu Rev Physiol, 60, 243, 10.1146/annurev.physiol.60.1.243 · DOI
- Konrad, 1994, Mucociliary transport in ICU patients, Chest, 105, 237, 10.1378/chest.105.1.237 · DOI
- Kress, 2009, Clin Ther, 31, 1177, 10.1016/j.clinthera.2009.05.022 · DOI
- Krishnamoorthy, 1998, Prodrugs for nasal drug delivery, Adv Drug Deliv Rev, 29, 135, 10.1016/S0169-409X(97)00065-3 · DOI
- Kundoor, 2011, Effect of formulation- and administration-related variables on deposition pattern of nasal spray pumps evaluated using a nasal cast, Pharm Res, 28, 1895, 10.1007/s11095-011-0417-6 · DOI
- Labiris, 2003, Pulmonary drug delivery. Part I: physiological factors affecting therapeutic effectiveness of aerosolized medications, Br J Clin Pharmacol, 56, 588, 10.1046/j.1365-2125.2003.01892.x · DOI
- Lennernas, 2010, Sublingual administration of fentanyl to cancer patients is an effective treatment for breakthrough pain: results from a randomized phase II study, Palliat Med, 24, 286, 10.1177/0269216309356138 · DOI
- Leow, 1992, Comparative oxycodone pharmacokinetics in humans after intravenous, oral, and rectal administration, Ther Drug Monit, 14, 479, 10.1097/00007691-199212000-00008 · DOI
- Leow, 1992, Single-dose and steady-state pharmacokinetics and pharmacodynamics of oxycodone in patients with cancer, Clin Pharmacol Ther, 52, 487, 10.1038/clpt.1992.176 · DOI · Paper page
- Lin, 2005, Transport of anti-allergic drugs across the passage cultured human nasal epithelial cell monolayer, Eur J Pharm Sci, 26, 203, 10.1016/j.ejps.2005.06.003 · DOI
- Liote, 1989, Role of mucus and cilia in nasal mucociliary clearance in healthy subjects, Am Rev Respir Dis, 140, 132, 10.1164/ajrccm/140.1.132 · DOI
- Loder, 2006, Post-marketing experience with an opioid nasal spray for migraine: lessons for the future, Cephalalgia, 26, 89, 10.1111/j.1468-2982.2005.00951.x · DOI
- Lofwall, 2012, Pharmacokinetics of intranasal crushed OxyContin and intravenous oxycodone in nondependent prescription opioid abusers, J Clin Pharmacol, 52, 600, 10.1177/0091270011401620 · DOI
- Loimer, 1992, Nasal administration of naloxone for detection of opiate dependence, J Psychiatr Res, 26, 39, 10.1016/0022-3956(92)90014-F · DOI
- Loimer, 1994, Nasal administration of naloxone is as effective as the intravenous route in opiate addicts, Int J Addict, 29, 819, 10.3109/10826089409047912 · DOI
- Lou, 1999, Delayed irradiation effects on nasal epithelium in patients with nasopharyngeal carcinoma. An ultrastructural study, Ann Otol Rhinol Laryngol, 108, 474, 10.1177/000348949910800510 · DOI
- Mathieu, 2006, Intranasal sufentanil is effective for postoperative analgesia in adults, Can J Anaesth, 53, 60, 10.1007/BF03021528 · DOI
- Matsuyama, 2006, Enhancement of nasal absorption of large molecular weight compounds by combination of mucolytic agent and nonionic surfactant, J Control Release, 110, 347, 10.1016/j.jconrel.2005.09.047 · DOI
- Matsuyama, 2006, Improved nasal absorption of salmon calcitonin by powdery formulation with N-acetyl-L-cysteine as a mucolytic agent, J Control Release, 115, 183, 10.1016/j.jconrel.2006.08.004 · DOI
- McCarberg, 2007, The treatment of breakthrough pain, Pain Med, 8, S8, 10.1111/j.1526-4637.2006.00270.x · DOI
- McMartin, 1987, Analysis of structural requirements for the absorption of drugs and macromolecules from the nasal cavity, J Pharm Sci, 76, 535, 10.1002/jps.2600760709 · DOI
- Meijer, 1999, Transport mechanisms for cationic drugs and proteins in kidney, liver and intestine: implication for drug interactions and cell-specific drug delivery, Nephrol Dial Transplant, 14, 1, 10.1093/ndt/14.suppl_4.1b · DOI
- Mercadante, 2009, A comparison of intranasal fentanyl spray with oral transmucosal fentanyl citrate for the treatment of breakthrough cancer pain: an open-label, randomised, crossover trial, Curr Med Res Opin, 25, 2805, 10.1185/03007990903336135 · DOI
- Mercadante, 2007, Transmucosal fentanyl vs intravenous morphine in doses proportional to basal opioid regimen for episodic-breakthrough pain, Br J Cancer, 96, 1828, 10.1038/sj.bjc.6603811 · DOI
- Middleton, 1993, Effect of amiloride and saline on nasal mucociliary clearance and potential difference in cystic fibrosis and normal subjects, Thorax, 48, 812, 10.1136/thx.48.8.812 · DOI
- Miller, 2008, Comparison of intranasal administration of haloperidol with intravenous and intramuscular administration: a pilot pharmacokinetic study, Pharmacotherapy, 28, 875, 10.1592/phco.28.7.875 · DOI
- Mizuno, 2003, Impact of drug transporter studies on drug discovery and development, Pharmacol Rev, 55, 425, 10.1124/pr.55.3.1 · DOI
- Moksnes, 2008, Early pharmacokinetics of nasal fentanyl: is there a significant arterio-venous difference?, Eur J Clin Pharmacol, 64, 497, 10.1007/s00228-007-0444-8 · DOI
- Morimoto, 1991, Effects of proteolytic enzyme inhibitors on the nasal absorption of vasopressin and an analogue, Pharm Res, 8, 1175, 10.1023/A:1015862603939 · DOI
- Morrison, 1990, Morphology of the human olfactory epithelium, J Comp Neurol, 297, 1, 10.1002/cne.902970102 · DOI
- Newman, 1987, Deposition pattern from a nasal pump spray, Rhinology, 25, 77
- Newman, 1994, The distribution of an intranasal insulin formulation in healthy volunteers: effect of different administration techniques, J Pharm Pharmacol, 46, 657, 10.1111/j.2042-7158.1994.tb03877.x · DOI
- O'Brien, 2012, Interactions between antidepressants and P-glycoprotein at the blood–brain barrier: clinical significance of in vitro and in vivo findings, Br J Pharmacol, 165, 289, 10.1111/j.1476-5381.2011.01557.x · DOI
- Ohkubo, 1995, Human nasal mucosal carboxypeptidase: activity, location, and release, J Allergy Clin Immunol, 96, 924, 10.1016/S0091-6749(95)70230-X · DOI
- Ohkubo, 1994, Immunological localization of neuropeptide-degrading enzymes in the nasal mucosa, Rhinology, 32, 130
- Paech, 2003, A new formulation of nasal fentanyl spray for postoperative analgesia: a pilot study, Anaesthesia, 58, 740, 10.1046/j.1365-2044.2003.03286.x · DOI
- Parab, 1988, Pharmacokinetics of hydromorphone after intravenous, peroral and rectal administration to human subjects, Biopharm Drug Dispos, 9, 187, 10.1002/bod.2510090207 · DOI
- Pavis, 2002, Pilot study of nasal morphine–chitosan for the relief of breakthrough pain in patients with cancer, J Pain Symptom Manage, 24, 598, 10.1016/S0885-3924(02)00522-5 · DOI
- Pereswetoff-Morath, 1998, Microspheres as nasal drug delivery systems, Adv Drug Deliv Rev, 29, 185, 10.1016/S0169-409X(97)00069-0 · DOI
- Portenoy, 2010, A multicenter, placebo-controlled, double-blind, multiple-crossover study of Fentanyl Pectin Nasal Spray (FPNS) in the treatment of breakthrough cancer pain, Pain, 151, 617, 10.1016/j.pain.2010.07.028 · DOI
- Portenoy, 1990, Breakthrough pain: definition, prevalence and characteristics, Pain, 41, 273, 10.1016/0304-3959(90)90004-W · DOI
- Raphael, 1996, Effects of 3 MAC of halothane, enflurane and isoflurane on cilia beat frequency of human nasal epithelium in vitro, Br J Anaesth, 76, 116, 10.1093/bja/76.1.116 · DOI
- Rauck, 2009, Efficacy and long-term tolerability of sublingual fentanyl orally disintegrating tablet in the treatment of breakthrough cancer pain, Curr Med Res Opin, 25, 2877, 10.1185/03007990903368310 · DOI
- Robbins, 1993, Stadol Nasal Spray—treatment for migraine?, Headache, 33, 220
- Rudy, 2004, A multiple-dose phase I study of intranasal hydromorphone hydrochloride in healthy volunteers, Anesth Analg, 99, 1379, 10.1213/01.ANE.0000132927.47528.8B · DOI
- Sachdeva, 1993, Nasal mucociliary clearance & mucus pH in patients with diabetes mellitus, Indian J Med Res, 98, 265
- Salib, 2008, Mechanisms and mediators of nasal symptoms in non-allergic rhinitis, Clin Exp Allergy, 38, 393, 10.1111/j.1365-2222.2007.02926.x · DOI
- Salzman, 1995, Nitric oxide dilates tight junctions and depletes ATP in cultured Caco-2BBe intestinal epithelial monolayers, Am J Physiol, 268, G361
- Scheibe, 2008, Intranasal administration of drugs, Arch Otolaryngol Head Neck Surg, 134, 643, 10.1001/archotol.134.6.643 · DOI
- Schwagmeier, 1995, Pharmacokinetics of intranasal alfentanil, J Clin Anesth, 7, 109, 10.1016/0952-8180(94)00023-W · DOI
- Selwyn, 1996, Effects of morphine on human nasal cilia beat frequency in vitro, Br J Anaesth, 76, 274, 10.1093/bja/76.2.274 · DOI
- Shao, 1992, Cyclodextrins as nasal absorption promoters of insulin: mechanistic evaluations, Pharm Res, 9, 1157, 10.1023/A:1015847604654 · DOI
- Shyu, 1996, Pharmacokinetics of butorphanol nasal spray in patients with renal impairment, Br J Clin Pharmacol, 41, 397, 10.1046/j.1365-2125.1996.03327.x · DOI
- Shyu, 1993, Multiple-dose phase I study of transnasal butorphanol, Clin Pharmacol Ther, 54, 34, 10.1038/clpt.1993.106 · DOI
- Shyu, 1993, The absolute bioavailability of transnasal butorphanol in patients experiencing rhinitis, Eur J Clin Pharmacol, 45, 559, 10.1007/BF00315315 · DOI
- Simon, 1977, Measurement of transport in mucous membrane in the human nose with Cr-51-labeled resin beads, Acta Otolaryngol, 83, 378, 10.3109/00016487709128860 · DOI
- Soane, 1999, Evaluation of the clearance characteristics of bioadhesive systems in humans, Int J Pharm, 178, 55, 10.1016/S0378-5173(98)00367-6 · DOI
- Stanley, 1986, Effect of cigarette smoking on nasal mucociliary clearance and ciliary beat frequency, Thorax, 41, 519, 10.1136/thx.41.7.519 · DOI
- Stoker, 2008, Analgesic efficacy and safety of morphine–chitosan nasal solution in patients with moderate to severe pain following orthopedic surgery, Pain Med, 9, 3, 10.1111/j.1526-4637.2007.00300.x · DOI
- Striebel, 1993, Pharmacokinetics of intranasal Fentanyl, Schmerz, 7, 122, 10.1007/BF02527870 · DOI
- Stringer, 1995, Nasal mucociliary clearance after radiation therapy, Laryngoscope, 105, 380, 10.1288/00005537-199504000-00008 · DOI
- Surico, 2001, Impairment of nasal mucociliary clearance after radiotherapy for childhood head cancer, Head Neck, 23, 461, 10.1002/hed.1060 · DOI
- Tachibana, 2010, Predicting drug–drug interactions involving the inhibition of intestinal CYP3A4 and P-glycoprotein, Curr Drug Metab, 11, 762, 10.2174/138920010794328922 · DOI
- Takala, 1997, Pharmacokinetic comparison of intravenous and intranasal administration of oxycodone, Acta Anaesthesiol Scand, 41, 309, 10.1111/j.1399-6576.1997.tb04684.x · DOI
- Tetko, 2005, Virtual computational chemistry laboratory—design and description, J Comput Aided Mol Des, 19, 453, 10.1007/s10822-005-8694-y · DOI
- Vachharajani, 1996, The absolute bioavailability and pharmacokinetics of butorphanol nasal spray in patients with hepatic impairment, Clin Pharmacol Ther, 60, 283, 10.1016/S0009-9236(96)90055-7 · DOI
- Vachharajani, 1997, The pharmacokinetics of butorphanol and its metabolites at steady state following nasal administration in humans, Biopharm Drug Dispos, 18, 191, 10.1002/(SICI)1099-081X(199704)18:3<191::AID-BDD9>3.0.CO;2-6 · DOI
- Vachharajani, 2002, A pharmacokinetic interaction study between butorphanol and sumatriptan nasal sprays in healthy subjects: importance of the timing of butorphanol administration, Cephalalgia, 22, 282, 10.1046/j.1468-2982.2002.00359.x · DOI
- Veldhorst-Janssen, 2010, Clin Ther, 32, 1427, 10.1016/j.clinthera.2010.07.001 · DOI
- Verghese, 2008, The effect of intranasal administration of remifentanil on intubating conditions and airway response after sevoflurane induction of anesthesia in children, Anesth Analg, 107, 1176, 10.1213/ane.0b013e3181838e95 · DOI
- Wanner, 1996, Mucociliary clearance in the airways, Am J Respir Crit Care Med, 154, 1868, 10.1164/ajrccm.154.6.8970383 · DOI
- Washington, 2000, Determination of baseline human nasal pH and the effect of intranasally administered buffers, Int J Pharm, 198, 139, 10.1016/S0378-5173(99)00442-1 · DOI
- Watts, 2009, PecSys: in situ gelling system for optimised nasal drug delivery, Expert Opin Drug Deliv, 6, 543, 10.1517/17425240902939135 · DOI
- Wermeling, 2005, Analgesic effects of intranasal butorphanol tartrate administered via a unit-dose device in the dental impaction pain model: a randomized, double-blind, placebo-controlled, parallel-group study, Clin Ther, 27, 430, 10.1016/j.clinthera.2005.04.002 · DOI
- Wermeling, 2001, Bioavailability and pharmacokinetics of lorazepam after intranasal, intravenous, and intramuscular administration, J Clin Pharmacol, 41, 1225, 10.1177/00912700122012779 · DOI
- Wermeling, 2005, Pharmacokinetics, bioequivalence, and spray weight reproducibility of intranasal butorphanol after administration with 2 different nasal spray pumps, J Clin Pharmacol, 45, 969, 10.1177/0091270005278057 · DOI
- Westerling, 1995, Plasma concentrations of morphine, morphine-3-glucuronide, and morphine-6-glucuronide after intravenous and oral administration to healthy volunteers: relationship to nonanalgesic actions, Ther Drug Monit, 17, 287, 10.1097/00007691-199506000-00013 · DOI
- Wioland, 2000, CFTR, MDR1, and MRP1 immunolocalization in normal human nasal respiratory mucosa, J Histochem Cytochem, 48, 1215, 10.1177/002215540004800905 · DOI
- Yang, 2001, Chemical stability, enzymatic hydrolysis, and nasal uptake of amino acid ester prodrugs of acyclovir, J Pharm Sci, 90, 617, 10.1002/1520-6017(200105)90:5<617::AID-JPS1018>3.0.CO;2-5 · DOI
- Zaki, 2006, Rapid-onset intranasal delivery of metoclopramide hydrochloride. Part I. Influence of formulation variables on drug absorption in anesthetized rats, Int J Pharm, 327, 89, 10.1016/j.ijpharm.2006.07.040 · DOI
- Zedie, 1996, Comparison of intranasal midazolam and sufentanil premedication in pediatric outpatients, Clin Pharmacol Ther, 59, 341, 10.1016/S0009-9236(96)80012-9 · DOI
- Zeppetella, 2000, An assessment of the safety, efficacy, and acceptability of intranasal fentanyl citrate in the management of cancer-related breakthrough pain: a pilot study, J Pain Symptom Manage, 20, 253, 10.1016/S0885-3924(00)00180-9 · DOI
- Zeppetella, 2006, Opioids for the management of breakthrough (episodic) pain in cancer patients, Cochrane Database Syst Rev, CD004311
- Zhang, 2005, Expression of cytochrome p450 and other biotransformation genes in fetal and adult human nasal mucosa, Drug Metab Dispos, 33, 1423, 10.1124/dmd.105.005769 · DOI
Cited by
Sorted by citations
Agrawal, M., Saraf, S., Saraf, S., Antimisiaris, S. G., Chougule, M. B., Shoyele, S. A., & Alexander, A. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.05.011 · Cited by 630
Guastella, A. J., Hickie, I. B., McGuinness, M. M., Otis, M., Woods, E. A., Disinger, H. M., Chan, H.-K., Chen, T. F., & Banati, R. B. (2013) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.11.019 · Cited by 357
The Opioid Epidemic: Crisis and Solutions
Skolnick, P. (2018) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010617-052534 · Cited by 307
Swain, J. E., Kim, P., Spicer, J., Ho, S. S., Dayton, C. J., Elmadih, A., & Abel, K. M. (2014) · Brain Research · doi:10.1016/j.brainres.2014.03.007 · Cited by 290
Dendrimer-Based Drug Delivery Systems for Brain Targeting
Zhu, Y., Liu, C., & Pang, Z. (2019) · Biomolecules · doi:10.3390/biom9120790 · Cited by 220
Metadata
- Authors
- Grassin-Delyle, S., Buenestado, A., Naline, E., Faisy, C., Blouquit-Laye, S., Couderc, L.-J., Le Guen, M., Fischler, M., & Devillier, P.
- Venue
- Pharmacology & Therapeutics
- Publisher
- Elsevier BV
- Published
- 2012-06
- Volume
- 134
- Issue
- 3
- Pages
- 366-379
- ISSN
- 0163-7258
- Cited by
- 398
- References
- 3
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review