دورية أكاديمية
Atorvastatin-loaded nanostructured lipid carriers (NLCs): strategy to overcome oral delivery drawbacks
العنوان: | Atorvastatin-loaded nanostructured lipid carriers (NLCs): strategy to overcome oral delivery drawbacks |
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المؤلفون: | Mohammed Elmowafy, Hany M. Ibrahim, Mohammed A. Ahmed, Khaled Shalaby, Ayman Salama, Hossam Hefesha |
المصدر: | Drug Delivery, Vol 24, Iss 1, Pp 932-941 (2017) |
بيانات النشر: | Taylor & Francis Group, 2017. |
سنة النشر: | 2017 |
المجموعة: | LCC:Therapeutics. Pharmacology |
مصطلحات موضوعية: | atorvastatin, nanostructured lipid carriers (nlcs), oral delivery, bioavailability, pharmacodynamic effects, Therapeutics. Pharmacology, RM1-950 |
الوصف: | Atorvastatin (AT) is a widely used lipid-regulating drug to reduce cholesterol and triglycerides. Its poor aqueous solubility and hepatic metabolism require development of drug delivery systems able to improve its solubility and bypass hepatic effect. For this purpose, atorvastatin nanostructured lipid carriers (AT-NLCs) were prepared and characterized. AT-NLCs were prepared by emulsification using high-speed homogenization followed by ultrasonication. The prepared NLCs showed particle size between 162.5 ± 12 and 865.55 ± 28 nm while zeta potential values varied between −34 ± 0.29 and −23 ± 0.36 mV. They also showed high encapsulation efficiency (>87%) and amorphous state of the drug in lipid matrix. Pharmacokinetic parameters of optimized formulation (NLC-1; composed of 2% Gelucire® 43/01, 8% Capryol® PGMC, 2% Pluronic®F68 and 0.5% lecithin) revealed 3.6- and 2.1-fold increase in bioavailability as compared to atorvastatin suspension and commercial product (Lipitor®), respectively. Administration of NLC-1 led to significant reduction (p |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 1071-7544 1521-0464 10717544 |
Relation: | https://doaj.org/toc/1071-7544; https://doaj.org/toc/1521-0464 |
DOI: | 10.1080/10717544.2017.1337823 |
URL الوصول: | https://doaj.org/article/4404a11244aa460997ae26701fe5a17b |
رقم الأكسشن: | edsdoj.4404a11244aa460997ae26701fe5a17b |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 10717544 15210464 |
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DOI: | 10.1080/10717544.2017.1337823 |