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热熔挤出技术在盐酸伐昔洛韦眼用植入剂制备和评价中的新应用。

Novel Application of Hot Melt Extrusion Technology for Preparation and Evaluation of Valacyclovir Hydrochloride Ocular Inserts.

机构信息

Department of Pharmaceutics and Drug Delivery, Pii Center for Pharmaceutical Technology, School of Pharmacy, University of Mississippi, University, Mississippi, 38677, USA.

Pii Center for Pharmaceutical Technology, University of Mississippi, University, Mississippi, 38677, USA.

出版信息

AAPS PharmSciTech. 2021 Jan 14;22(1):48. doi: 10.1208/s12249-020-01916-5.

Abstract

The objective of this study was to investigate the processability of hot-melt extrusion (HME) to formulate ocular inserts of valacyclovir hydrochloride and evaluate the in vivo bioavailability of the formulation. To optimize the formulation of this drug, different physical mixtures of the polymers and plasticizer were prepared. The physical mixture was extruded through a co-rotating twin-screw extruder, and the obtained ocular inserts were cut with dimensions of 4 mm × 2 mm × 1 mm to enhance the formulation instillation in the eye. Ocular inserts were evaluated for drug content, weight variation, uniformity of thickness, in vitro drug release, and in vivo drug bioavailability. The ocular inserts were thermally characterized using differential scanning calorimetry (DSC). The attributes observed for the ocular inserts were within the target specifications. The ocular inserts of valacyclovir hydrochloride were successfully prepared using the HME. They provided sustained drug release along with enhanced drug permeation when compared with the eyedrop solution and dissolve completely in 8 h. Additionally, the obtained results demonstrated that the formulation of ocular inserts of valacyclovir hydrochloride using HME was reproducible, robust, and effective method.

摘要

本研究旨在探讨热熔挤出(HME)工艺来制备盐酸伐昔洛韦眼部插入剂,并评估该制剂的体内生物利用度。为了优化该药物的配方,制备了不同聚合物和增塑剂的物理混合物。将物理混合物通过同向旋转双螺杆挤出机挤出,然后将得到的眼部插入剂切割成 4mm×2mm×1mm 的尺寸,以增强药物在眼睛中的滴注。对眼部插入剂进行了药物含量、重量变化、厚度均匀性、体外药物释放和体内药物生物利用度的评价。使用差示扫描量热法(DSC)对眼部插入剂进行了热特性分析。眼部插入剂的各项属性均符合目标规格。成功地使用 HME 制备了盐酸伐昔洛韦眼部插入剂。与滴眼剂溶液相比,它们提供了持续的药物释放和增强的药物渗透,并且在 8 小时内完全溶解。此外,所得结果表明,使用 HME 制备盐酸伐昔洛韦眼部插入剂的配方是可重现、稳健且有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c40/7886274/6e58d5d932f6/nihms-1665296-f0001.jpg

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