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通过可注射原位形成温敏水凝胶制剂研究新型几乎不溶的美妥昔单抗诱导抗癌剂 5-甲氧基 MOMIPP 的体内递送和维持血浆及脑内水平的潜力。

Investigating the Potential to Deliver and Maintain Plasma and Brain Levels of a Novel Practically Insoluble Methuosis Inducing Anticancer Agent 5-Methoxy MOMIPP Through an Injectable In Situ Forming Thermoresponsive Hydrogel Formulation.

机构信息

Division of Industrial Pharmacy, Department of Pharmacy Practice, College of Pharmacy and Pharmaceutical Sciences, University of Toledo HSC, Toledo, Ohio 43614.

Department of Cancer Biology, College of Medicine and Life Sciences, University of Toledo HSC, Toledo, Ohio 43614.

出版信息

J Pharm Sci. 2020 Sep;109(9):2719-2728. doi: 10.1016/j.xphs.2020.05.014. Epub 2020 May 28.

DOI:10.1016/j.xphs.2020.05.014
PMID:32473210
Abstract

A new indole based chalcone molecule MOMIPP induced methuosis mediated cell death in gliobastoma and other cancer cell lines. But the drug was insoluble in water and had a very short plasma half-life. The purpose of this work was to develop a formulation that can provide sustained levels of MOMIPP in vivo. Initial studies established drug solubility in various solvents. N-methyl pyrrolidone (NMP) was determined as an excellent solvent for the drug. Subsequently a poloxamer-407 based thermoreversible gel containing NMP was used to develop the formulation. Rheological studies were performed via oscillatory temperature mode, continuous shear analysis, and oscillatory frequency mode experiments. The mechanical properties of the formulations were tested using a texture profile analyzer. The gelation temperature and time of formulations increased with increasing amounts of NMP. However, the viscosity at 20 °C and storage modulus decreased as the amount of NMP increased. Characterization studies helped to identify the gel formulation that was used to administer the drug orally, sub-cutaneously, and intra-peritoneally. When the gel was given intraperitoneally the target plasma and brain levels of over 5 μM was maintained for about 8 h. Thus, a thermoreversible gel formulation that can deliver MOMIPP in animal studies was successfully developed.

摘要

一种新型吲哚类查尔酮分子 MOMIPP 可诱导神经胶质母细胞瘤和其他癌细胞的自噬性细胞死亡。但该药物在水中不溶,血浆半衰期极短。本研究旨在开发一种能在体内提供持续 MOMIPP 水平的制剂。初步研究确定了药物在各种溶剂中的溶解度。N-甲基吡咯烷酮(NMP)被确定为药物的优良溶剂。随后,使用基于泊洛沙姆 407 的含 NMP 的温敏凝胶来开发制剂。通过振荡温度模式、连续剪切分析和振荡频率模式实验进行流变学研究。使用质地分析仪测试制剂的机械性能。制剂的胶凝温度和时间随 NMP 用量的增加而增加。然而,随着 NMP 用量的增加,20°C 时的粘度和储能模量降低。表征研究有助于确定用于口服、皮下和腹腔内给药的凝胶制剂。当凝胶经腹腔内给药时,目标血浆和大脑中的药物浓度超过 5μM 并能维持约 8 小时。因此,成功开发了一种可在动物研究中递送 MOMIPP 的温敏凝胶制剂。

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