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使用Strat-M膜评估制剂参数对布洛芬从局部用制剂中渗透的影响。

Evaluation of Formulation Parameters on Permeation of Ibuprofen from Topical Formulations Using Strat-M Membrane.

作者信息

Bolla Pradeep Kumar, Clark Bradley A, Juluri Abhishek, Cheruvu Hanumanth Srikanth, Renukuntla Jwala

机构信息

Department of Biomedical Engineering, College of Engineering, The University of Texas at El Paso, 500 W. University Ave, El Paso, TX 79968, USA.

Department of Basic Pharmaceutical Sciences, Fred Wilson School of Pharmacy, High Point University, High Point, NC 27268, USA.

出版信息

Pharmaceutics. 2020 Feb 13;12(2):151. doi: 10.3390/pharmaceutics12020151.

Abstract

Topical drug delivery is an attractive alternative to conventional methods because of advantages such as non-invasive delivery, by-pass of first pass metabolism, and improved patient compliance. However, several factors such as skin, physicochemical properties of the drug, and vehicle characteristics influence the permeation. Within a formulation, critical factors such as concentration of drug, physical state of drug in the formulation, and organoleptic properties affect the flux across the skin. The aim of the study was to develop and investigate topical semisolid preparations (creams and gels) with ibuprofen as the model drug and investigate the effect of various formulation parameters on the in-vitro performance across the Strat-M membrane using flow-through cells. In addition, the physical stability of the developed formulations was investigated by studying viscosity, pH, and appearance. All the formulations developed in the study had appealing appearance with smooth texture and no signs of separation. Viscosity and pH of the formulations were acceptable. Cumulative amount of drug permeated at the end of 24 h was highest for clear gel (3% / ibuprofen; F6: 739.6 ± 36.1 µg/cm) followed by cream with high concentration of ibuprofen in suspended form (5% /; F3: 320.8 ± 17.53 µg/cm), emulgel (3% / ibuprofen; F5: 178.5 ± 34.5 µg/cm), and cream with solubilized ibuprofen (3% /; F2A: 163.2 ± 9.36 µg/cm). Results from this study showed that permeation of ibuprofen was significantly influenced by formulation parameters such as concentration of ibuprofen (3% vs. 5% /), physical state of ibuprofen (solubilized vs. suspended), formulation type (cream vs. gel), mucoadhesive agents, and viscosity (high vs. low). Thus, findings from this study indicate that pharmaceutical formulation scientists should explore these critical factors during the early development of any new topical drug product in order to meet pre-determined quality target product profile.

摘要

由于具有非侵入性给药、避免首过代谢以及提高患者顺应性等优点,局部给药是传统给药方法的一种有吸引力的替代方式。然而,皮肤、药物的物理化学性质以及载体特性等几个因素会影响药物渗透。在一种制剂中,药物浓度、药物在制剂中的物理状态以及感官性质等关键因素会影响药物透过皮肤的通量。本研究的目的是以布洛芬为模型药物开发并研究局部半固体制剂(乳膏和凝胶),并使用流通池研究各种制剂参数对其透过Strat-M膜的体外性能的影响。此外,通过研究粘度、pH值和外观来考察所开发制剂的物理稳定性。本研究中开发的所有制剂外观均吸引人,质地光滑,无分离迹象。制剂的粘度和pH值均可接受。24小时结束时,透明凝胶(3%布洛芬;F6:739.6±36.1μg/cm²)的药物累积渗透量最高,其次是高浓度布洛芬悬浮形式的乳膏(5%;F3:320.8±17.53μg/cm²)、乳胶凝胶(3%布洛芬;F5:178.5±34.5μg/cm²)以及布洛芬增溶的乳膏(3%;F2A:163.2±9.36μg/cm²)。本研究结果表明,布洛芬的渗透受到制剂参数的显著影响,如布洛芬浓度(3%对5%)、布洛芬的物理状态(增溶对悬浮)、制剂类型(乳膏对凝胶)、粘膜粘附剂以及粘度(高对低)。因此,本研究结果表明,药物制剂科学家在任何新的局部药物产品的早期开发过程中应探索这些关键因素,以满足预先确定的质量目标产品概况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2554/7076669/b230c1f2ed16/pharmaceutics-12-00151-g001.jpg

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