Formulation and Evaluation of Metronidazole Loaded Nanosponges for Topical Delivery

Rashid A Khan, Dr. Anum Saif, Humaira Naureen, Atif Sarwar, Muhammad Ali Shahbaz, Muhammad Nouman Arif
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引用次数: 0

Abstract

Formulations of metronidazole M1, M2, M3, M4, and M5 with the polymer ethyl cellulose and M1*, M2*, M3*, M4* and M5* with the polymer Eudragit RS100 at varying concentrations were prepared and characterized by Zeta sizer, SEM, DSC, FTIR and XRD. The gel was evaluated for its spreadability, skin irritancy, entrapment efficiency and drug release. Size in M5* was 292.2 nm with PDI of 1.00 and in M2, 371.8 nm with PDI of 0.809 was observed. The entrapment efficiency and production yield with M5* was observed to be 68.40 % and 66.9 % respectively. While the EE and PY with M2 were 66.70 % and 58 % respectively. FTIR did not reveal any incompatibility between the polymer and the drugs and by SEM results, the shape of nanosponges appeared to be spherical and porous. 10% of the drug was released from nanosponges in Ist hour and almost 70 % in 8 hours.
外用甲硝唑纳米海绵的制备及评价
制备了甲硝唑M1、M2、M3、M4、M5与聚合物乙基纤维素和M1*、M2*、M3*、M4*、M5*与聚合物Eudragit RS100在不同浓度下的配方,并用Zeta浆料、SEM、DSC、FTIR和XRD对其进行了表征。对凝胶的涂抹性、皮肤刺激性、包封效率和药物释放进行了评价。M5*的尺寸为292.2 nm, PDI为1.00;M2的尺寸为371.8 nm, PDI为0.809。M5*的捕集效率和产量分别为68.40%和66.9%。M2的EE和PY分别为66.70%和58%。FTIR未发现聚合物与药物之间存在不相容性,SEM结果显示纳米海绵呈球形和多孔状。纳米海绵在1小时内释放10%的药物,在8小时内释放近70%的药物。
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