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紫杉醇纳米混悬剂用于靶向化疗 - 纳米混悬剂的制备、表征和应用。

Paclitaxel nanosuspensions for targeted chemotherapy - nanosuspension preparation, characterization, and use.

机构信息

Baxter Healthcare Corporation , Round Lake, IL , USA and.

出版信息

Pharm Dev Technol. 2014 Jun;19(4):438-53. doi: 10.3109/10837450.2013.789911. Epub 2013 Apr 25.

Abstract

OBJECTIVE

The purpose of this work was to prepare a stable paclitaxel nanosuspension and test it for potential use as a targeted chemotherapeutic. Different particle coatings were employed to assess their impact on cellular uptake in vitro. In vivo work was then performed to demonstrate efficacy in tumor-bearing mouse models.

MATERIALS AND METHOD

Paclitaxel nanosuspensions were prepared using a homogenization process and coated with excipients. Surface charge was measured by zeta potential, potency by high-performance liquid chromatography, and solubility using an in-line UV probe. Cellular uptake studies were performed via flow cytometry. In vivo experiments were performed to determine residence time, maximum tolerated dose, and the efficacy of paclitaxel nanosuspensions (Paclitaxel-NS).

RESULTS

A stable paclitaxel nanosuspension was prepared and coated with various excipients. Studies in mice showed that the nanosuspension was well-tolerated and at least as effective as the IV Taxol control in prolonging mouse survival in a head and neck cancer model as well as an ovarian cancer model with a lower overall drug dose than the traditional IV administration route.

CONCLUSIONS

The paclitaxel nanosuspension is suitable for cellular uptake. The nanosuspension was effective in prolonging life in two separate xenograft orthotopic murine cancer models through two separate routes of administration.

摘要

目的

本研究旨在制备稳定的紫杉醇纳米混悬剂,并评估其作为靶向化疗药物的潜力。采用不同的粒子包衣方法,考察其对细胞摄取的影响。然后在荷瘤小鼠模型中进行体内实验,以验证其疗效。

材料与方法

采用匀化法制备紫杉醇纳米混悬剂,并对其进行辅料包衣。通过zeta 电位测定表面电荷,高效液相色谱法测定药物含量,在线紫外探针法测定溶解度。采用流式细胞术进行细胞摄取研究。进行体内实验,以确定紫杉醇纳米混悬剂(紫杉醇纳米粒)的体内滞留时间、最大耐受剂量和疗效。

结果

成功制备了稳定的紫杉醇纳米混悬剂,并对其进行了不同辅料的包衣。在小鼠体内实验中,纳米混悬剂具有良好的耐受性,在延长头颈部肿瘤模型和卵巢癌模型小鼠生存期方面至少与 IV 紫杉醇对照组等效,且药物总剂量低于传统 IV 给药途径。

结论

紫杉醇纳米混悬剂适合细胞摄取。纳米混悬剂通过两种不同的给药途径,在两种独立的异种移植原位小鼠肿瘤模型中均能有效延长生存期。

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