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新型载链霉素和双氯芬酸的伤口愈合膜敷料的制备、优化和特性研究。

Preparation, optimisation and characterisation of novel wound healing film dressings loaded with streptomycin and diclofenac.

机构信息

Department of Pharmaceutical, Chemical and Environmental Sciences, School of Science, University of Greenwich at Medway, Central Avenue, Chatham Maritime, ME4 4TB, Kent, UK.

出版信息

Colloids Surf B Biointerfaces. 2013 Feb 1;102:102-10. doi: 10.1016/j.colsurfb.2012.08.014. Epub 2012 Aug 19.

Abstract

Streptomycin (STP) and diclofenac (DLF) loaded film dressings were prepared by blending Polyox(®) (POL) with four hydrophilic polymers [hydroxypropylmethylcellulose (HPMC), carrageenan (CAR), sodium alginate (SA) or chitosan (CS)] using glycerol (GLY) as plasticiser. The films were characterised by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy, texture analysis (tensile and swelling characteristics) and in vitro dissolution profiles using Franz diffusion cell. SEM showed homogeneous morphology for both blank (BLK) and drug loaded (DL) films. Films prepared by blending of POL with the other polymers showed a reduction in the crystallisation of POL in descending order of SA>CS>HPMC>CAR respectively. DSC and XRD showed no crystalline peaks of STP and DLF suggesting molecular dispersion of both drugs as well as possible drug interaction with negatively charged sulphate ions present in CAR. The DL films did not show any IR bands of both drugs, confirming the DSC and XRD results. POL-CAR-BLK films showed higher tensile strength (12.32±1.40 MPa) than the POL-CAR-DL films (9.52±1.12 MPa). DL films plasticised with 25%w/w GLY revealed soft and tough (tensile strength 1.02±0.28 MPa, % elongation 1031.33±16.23) formulations. The swelling capacities of POL-CAR-BLK and POL-CAR-DL films were (733.17±25.78%) and (646.39±40.39%), increasing to (1072.71±80.30%) and (1051±86.68%) for POL-CAR-BLK-25% GLY and POL-CAR-DL-25% GLY respectively. POL-CAR-DL films showed significantly (n=3, p<0.0318) lower cumulative release of STP and DLF (52.11±1.34, 55.26±2.25) compared to POL-CAR-DL-25% GLY films (60.07±1.56, 63.39±1.92) respectively.

摘要

链霉素(STP)和双氯芬酸(DLF)载药膜是通过将聚氧化(®)(POL)与四种亲水性聚合物[羟丙基甲基纤维素(HPMC)、卡拉胶(CAR)、海藻酸钠(SA)或壳聚糖(CS)]混合,并用甘油(GLY)作为增塑剂制备而成。通过扫描电子显微镜(SEM)、差示扫描量热法(DSC)、X 射线衍射(XRD)和傅里叶变换红外(FTIR)光谱、质地分析(拉伸和溶胀特性)和 Franz 扩散池中的体外溶解曲线对薄膜进行了表征。SEM 显示空白(BLK)和载药(DL)薄膜均具有均匀的形态。通过 POL 与其他聚合物共混制备的薄膜,SA>CS>HPMC>CAR 的顺序,POL 的结晶度降低。DSC 和 XRD 显示 STP 和 DLF 均没有结晶峰,表明两种药物均为分子分散,并且可能与 CAR 中带负电荷的硫酸根离子发生药物相互作用。DL 薄膜没有显示出两种药物的任何 IR 带,这证实了 DSC 和 XRD 的结果。POL-CAR-BLK 薄膜显示出比 POL-CAR-DL 薄膜更高的拉伸强度(12.32±1.40 MPa)(9.52±1.12 MPa)。含有 25%w/w GLY 的 DL 薄膜显示出柔软和坚韧的特性(拉伸强度为 1.02±0.28 MPa,伸长率为 1031.33±16.23%)。POL-CAR-BLK 和 POL-CAR-DL 薄膜的溶胀能力分别为(733.17±25.78%)和(646.39±40.39%),对于 POL-CAR-BLK-25% GLY 和 POL-CAR-DL-25% GLY 分别增加至(1072.71±80.30%)和(1051±86.68%)。与 POL-CAR-DL-25% GLY 薄膜相比,POL-CAR-DL 薄膜显示出显著(n=3,p<0.0318)较低的 STP 和 DLF 累积释放率(52.11±1.34,55.26±2.25),(60.07±1.56,63.39±1.92)。

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