首页> 外文期刊>Journal of pharmaceutical investigation >Formulation optimization of PVA/HPMC cryogel of Diltiazem HCl using 3-level factorial design and evaluation for ex vivo permeation
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Formulation optimization of PVA/HPMC cryogel of Diltiazem HCl using 3-level factorial design and evaluation for ex vivo permeation

机译:盐酸地尔硫卓的PVA / HPMC冷冻凝胶的三级因子设计和离体渗透评估的配方优化

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The aim of the present research was to optimize cryogel formulation of Diltiazem hydrochloride (DZ) with poly(vinyl alcohol) (PVA) and hydroxypropyl methylcellulose (HPMC) by utilizing response surface methodology followed by ex vivo permeation study on the optimized gel containing penetration enhancers. A 3-level factorial design was employed to formulate the experimental runs and to evaluate the effect of two independent variables such as the concentration of PVA and HPMC on characteristics of cryogel such as bioadhesive strength (BS) and in vitro drug release (dependent variables). Response surface plots such as contour and 3D plots were generated by the Design Expert? software to analyze the effect of independent variables on dependent variables. Fourier transform infrared spectroscopy studies confirmed the absence of interaction between DZ and polymers. Among various models generated by the software, quadratic model was found to be best fit for both the responses. Both the formulation factors influenced BS synergistically. However, the effect of HPMC concentration was more pronounced compared to concentration of PVA. But, an opposite effect shown by both the formulation factors on cumulative percentage of drug release (CPR) in 8 h. The optimized batch of cryogel of DZ selected by the software was having composition of 5 % of PVA and 2 % of HPMC. Penetration enhancers such as 1,8-cineole, d-limonene and carvone were incorporated into the optimized gel and permeation study was carried out using abdominal skin of rat. The study demonstrated a highest flux of 118 ± 5.81 μg/cm2/h in case of 1,8-cineole containing gel followed by carvone and d-limonene.
机译:本研究的目的是通过利用响应面法,然后在离体渗透研究中对含有渗透增强剂的优化凝胶进行体外优化,以优化盐酸地尔硫卓(DZ)与聚乙烯醇(PVA)和羟丙基甲基纤维素(HPMC)的冷冻凝胶配方。 。采用三级因子设计来制定实验运行并评估两个独立变量(例如PVA和HPMC的浓度)对冷冻凝胶特性(例如生物粘附强度(BS)和体外药物释放)的影响(因变量) 。响应曲面图(例如轮廓图和3D图)是由Design Expert?软件分析自变量对因变量的影响。傅里叶变换红外光谱研究证实了DZ和聚合物之间不存在相互作用。在该软件生成的各种模型中,发现二次模型最适合这两种响应。两种配方因素均协同影响BS。但是,与PVA浓度相比,HPMC浓度的影响更为明显。但是,两种配方因子对8小时内药物释放累积百分比(CPR)均显示相反的作用。通过软件选择的优化的DZ冷冻凝胶批次具有5%的PVA和2%的HPMC。将渗透促进剂如1,8-桉树脑,d-柠檬烯和香芹酮掺入优化的凝胶中,并使用大鼠的腹部皮肤进行渗透研究。该研究表明,在含有1,8-桉树脑的凝胶之后,香芹酮和d-柠檬烯的最高通量为118±5.81μg/ cm2 / h。

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