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2
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Int J Pharm Investig. 2011 Jan;1(1):42-7. doi: 10.4103/2230-973X.76728.
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Manufacture and characterization of mucoadhesive buccal films.黏膜粘附口腔膜的制备与特性研究。
Eur J Pharm Biopharm. 2011 Feb;77(2):187-99. doi: 10.1016/j.ejpb.2010.11.023. Epub 2010 Dec 3.
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Formulation and characterization of mucoadhesive buccal films of glipizide.格列吡嗪黏膜黏附性口腔膜剂的制剂与表征
Indian J Pharm Sci. 2008 Jan;70(1):43-8. doi: 10.4103/0250-474X.40330.
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Preparation and evaluation of buccoadhesive films of atenolol.阿替洛尔口腔黏附膜的制备与评价
Indian J Pharm Sci. 2008 Mar-Apr;70(2):175-9. doi: 10.4103/0250-474X.41451.
7
Buccoadhesive gels of glibenclamide: a means for achieving enhanced bioavailability.格列本脲的颊黏附凝胶:提高生物利用度的一种手段。
Drug Deliv. 2009 Oct;16(7):405-15. doi: 10.1080/10717540903126314.
8
Development and in vitro evaluation of floating rosiglitazone maleate microspheres.马来酸罗格列酮漂浮微球的研制及体外评价。
Drug Dev Ind Pharm. 2009 Jul;35(7):834-42. doi: 10.1080/03639040802627421.
9
Formulation, evaluation, and comparison of bilayered and multilayered mucoadhesive buccal devices of propranolol hydrochloride.盐酸普萘洛尔双层和多层黏膜黏附口腔制剂的制备、评价及比较
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10
Preparation and evaluation of a novel buccal adhesive system.一种新型口腔黏附系统的制备与评价
AAPS PharmSciTech. 2004 Apr 29;5(3):e35. doi: 10.1208/pt050335.

比较多孔与非多孔黏膜粘附性薄膜作为格列本脲颊部给药系统的效果。

Comparative evaluation of porous versus nonporous mucoadhesive films as buccal delivery system of glibenclamide.

机构信息

Department of Pharmaceutics, Rajiv Academy for Pharmacy, P.O. Chattikara, Mathura, 281001, Uttar Pradesh, India.

出版信息

AAPS PharmSciTech. 2013 Dec;14(4):1321-32. doi: 10.1208/s12249-013-0014-6. Epub 2013 Aug 30.

DOI:10.1208/s12249-013-0014-6
PMID:23990119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3840781/
Abstract

The present research work focused on the comparative assessment of porous versus nonporous films in order to develop a suitable buccoadhesive device for the delivery of glibenclamide. Both films were prepared by solvent casting technique using the 3(2) full factorial design, developing nine formulations (F1-F9). The films were evaluated for ex vivo mucoadhesive force, ex vivo mucoadhesion time, in vitro drug release (using a modified flow-through drug release apparatus), and ex vivo drug permeation. The mucoadhesive force, mucoadhesion time, swelling index, and tensile strength were observed to be directly proportional to the content of HPMC K4M. The optimized porous film (F4) showed an in vitro drug release of 84.47 ± 0.98%, ex vivo mucoadhesive force of 0.24 ± 0.04 N, and ex vivo mucoadhesion time of 539.11 ± 3.05 min, while the nonporous film (NF4) with the same polymer composition showed a release of 62.66 ± 0.87%, mucoadhesive force of 0.20 ± 0.05 N, and mucoadhesive time of 510 ± 2.00 min. The porous film showed significant differences for drug release and mucoadhesion time (p < 0.05) versus the nonporous film. The mechanism of drug release was observed to follow non-Fickian diffusion (0.1 < n < 0.5) for both porous and nonporous films. Ex vivo permeation studies through chicken buccal mucosa indicated improved drug permeation in porous films versus nonporous films. The present investigation established porous films to be a cost-effective buccoadhesive delivery system of glibenclamide.

摘要

本研究工作集中于多孔与非多孔薄膜的比较评估,以便开发适用于格列本脲传递的颊黏膜粘附制剂。两种薄膜均通过溶剂浇铸技术,使用 3(2)完全析因设计,制备了九种配方(F1-F9)。对薄膜进行了体外粘膜粘附力、体外粘膜粘附时间、体外药物释放(使用改良的流通药物释放装置)和体外药物渗透的评估。观察到粘膜粘附力、粘膜粘附时间、溶胀指数和拉伸强度与 HPMC K4M 的含量成正比。优化的多孔薄膜(F4)显示出 84.47±0.98%的体外药物释放、0.24±0.04 N 的体外粘膜粘附力和 539.11±3.05 min 的体外粘膜粘附时间,而具有相同聚合物组成的非多孔薄膜(NF4)则显示出 62.66±0.87%的释放、0.20±0.05 N 的粘膜粘附力和 510±2.00 min 的粘膜粘附时间。与非多孔薄膜相比,多孔薄膜在药物释放和粘膜粘附时间方面表现出显著差异(p<0.05)。观察到药物释放的机制对于多孔和非多孔薄膜均遵循非 Fickian 扩散(0.1<n<0.5)。通过鸡颊黏膜的体外渗透研究表明,多孔薄膜与非多孔薄膜相比,药物渗透得到了改善。本研究确立了多孔薄膜作为格列本脲颊黏膜粘附传递的一种具有成本效益的制剂。