RETRACTED: Development and Evaluation of in-situ Nasal Gel Formulations of Nanosized Transferosomal Sumatriptan: Design, Optimization, in vitro and in vivo Evaluation (Retracted article. See vol. 16, pg. 2291, 2022)

被引:40
|
作者
Omar, Mahmoud M. [1 ,2 ]
Eleraky, Nermin E. [3 ]
El Sisi, Amani M. [4 ]
Hasan, Omiya Ali [1 ,2 ]
机构
[1] Deraya Univ, Dept Pharmaceut & Ind Pharm, El Minia, Egypt
[2] Sohag Univ, Dept Pharmaceut, Sohag, Egypt
[3] Assiut Univ, Fac Pharm, Assiut, Egypt
[4] Beni Suef Univ, Dept Pharmaceut & Ind Pharm, Bani Suwayf, Egypt
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2019年 / 13卷
关键词
nanotransferosomes; sumatriptan succinate; SUT; thermosensitive in-situ gel and intranasal drug delivery system; TRANSDERMAL DELIVERY; SKIN PENETRATION; ACETAMINOPHEN; NANOVESICLES; NANOCAPSULES; RESVERATROL; ENHANCEMENT; TEMPERATURE; PREVALENCE; LIPOSOMES;
D O I
10.2147/DDDT.S235004
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Sumatriptan succinate (SUT) is a potent drug used for relieving or ending migraine and cluster headaches. SUT bioavailability is low (15%) when it is taken orally owing to its gastric breakdown and bloodstream before reaching the target arteries. Aim: The aim of the study was to enhance SUT bioavailability through developing an intranasal transferosomal mucoadhesive gel. Methods: SUT-loaded nanotransferosomes were prepared by thin film hydration method and characterized for various parameters such as vesicle diameter, percent entrapment efficiency (%EE), in vitro release and ex vivo permeation studies. The in-situ gels were prepared using various ratios of poloxamer 407, poloxamer 188, and carrageenan and characterized for gelation temperature, mucoadhesive strength, and rheological properties. Results: The prepared transferosomes exhibited percent entrapment efficiencies (%EE) of 40.41 +/- 3.02 to 77.47 +/- 2.85%, mean diameters of 97.25 to 245.01 nm, sustained drug release over 6 hours, and acceptable ex vivo permeation findings. The optimum formulae were incorporated into poloxamer 407 and poloxamer 188-based thermosensitive in-situ gel using carrageenan as a mucoadhesive polymer. Pharmacokinetic evaluation showed that the prepared in-situ gel of SUT-loaded nano-transferosomes gave enhanced bioavailability, 4.09-fold, as compared to oral drug solution. Conclusion: Based on enhancing the bioavailability and sustaining the drug release, it can be concluded that the in-situ gel of SUT-loaded nano-transferosomes were developed as a promising non-invasive drug delivery system for treating migraine.
引用
收藏
页码:4413 / 4430
页数:18
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