Cited by 158Advanced Drug Delivery SystemsNanoparticle-Based Drug DeliveryAdvancements in Transdermal Drug Delivery

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Comparison of ciprofloxacin hydrochloride‐loaded protein, lipid, and chitosan nanoparticles for drug delivery

Jain, Dharmendra, Banerjee, R.·2008·Journal of Biomedical Materials Research Part B: Applied Biomaterials

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Abstract

The aim of the present study was to develop single dose delivery systems based on nanotechnology for prolonged antibiotic release in a controlled manner. Five different drug–carrier ratios of ciprofloxacin hydrochloride‐loaded nanoparticles of albumin, gelatin, chitosan (CS), and lipid [solid lipid nanoparticles (SLNs)] were prepared and characterized. Average particle size was found to be in the range of 73 ± 2 to 98 ± 44 nm for SLNs, 140 ± 7 to 175 ± 24 nm for albumin nanoparticles, 143 ± 18 to 184 ± 27 nm for gelatin nanoparticles, and 247 ± 48 to 322 ± 52 nm for CS nanoparticles. A drug‐to‐carrier ratio of 0.5:1 was preferred for CS nanoparticles having zeta potential of >20 mV and drug encapsulation of 35.01% ± 2.66%. Similarly, 0.6:1 ratio was preferred for albumin nanoparticles with zeta potential >16 mV and drug encapsulation 48.20% ± 3.01%. Zeta potentials of gelatin nanoparticles loaded with ciprofloxacin suggested that they were unstable and prone to flocculation. SLN with 0.25:1 drug carrier ratio showed 38.71% ± 2.38% drug entrapment and −28 ± 1 mV surface charge. All the nanoparticles showed sustained drug release avoiding “burst effect” of the free drugs for up to 120 h for albumin nanoparticles, 96 h for CS and gelatin nanoparticles, and 80 h for SLNs. The drug release profiles followed Higuchi model. Results suggest that CS nanoparticles and SLNs can act as promising carriers for sustained ciprofloxacin release in infective conditions. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008

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Authors: Jain, D., & Banerjee, R.
Affiliations: Indian Institute of Technology Bombay (IN)
Corresponding author: Banerjee, R.
ORCID: Jain, Dharmendra
Banerjee, R.
Venue: Journal of Biomedical Materials Research Part B: Applied Biomaterials
Publisher: Wiley
Published: 2007-12-20
Volume: 86B
Issue: 1
Pages: 105-112
ISSN: 1552-4973 (ISSN-L)
1552-4981
DOI: 10.1002/jbm.b.30994
OpenAlex: W2074420216
Cited by: 158
References: 34
Citations by year: 2025: 6 · 2024: 7 · 2023: 7 · 2022: 9 · 2021: 14 · 2020: 11 · 2019: 15 · 2018: 12 · 2017: 18 · 2016: 15 · 2015: 7 · 2014: 5 · 2013: 11 · 2012: 4
FWCI: 3.11
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Journal of Biomedical Materials Research Part B Applied Biomaterials (publishedVersion)
PubMed (publishedVersion)
DSpace (IIT Bombay) (submittedVersion)
Topics: Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
Keywords: ciprofloxacin hydrochloride, chitosan nanoparticles, solid lipid nanoparticles, albumin nanoparticles, gelatin nanoparticles, sustained drug release, encapsulation efficiency, zeta potential, Higuchi model, burst release, nanoparticle stability
MeSH terms: Albumins, Animals, Cattle, Ciprofloxacin, Drug Carriers, Gelatin, Lipids, Particle Size, Polymers, Scattering, Radiation, Serum Albumin, Drug Delivery Systems, Nanotechnology, Chitosan, Nanoparticles

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Comparison of ciprofloxacin hydrochloride‐loaded protein, lipid, and chitosan nanoparticles for drug delivery

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