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将机械化学与喷雾凝结相结合,为血吸虫病治疗开发新的吡喹酮儿科制剂。

Combining Mechanochemistry and Spray Congealing for New Praziquantel Pediatric Formulations in Schistosomiasis Treatment.

机构信息

Department of Pharmacy and BioTechnology, University of Bologna, Via S. Donato 19/2, 40127 Bologna, Italy.

Department of Chemical and Pharmaceutical Sciences, University of Trieste, P.le Europa 1, 34127 Trieste, Italy.

出版信息

Int J Mol Sci. 2019 Mar 12;20(5):1233. doi: 10.3390/ijms20051233.

Abstract

Praziquantel (PZQ) is the first line drug for the treatment of schistosome infections and is included in the WHO Model List of Essential Medicines for Children. In this study, the association of mechanochemical activation (MA) and the spray congealing (SC) technology was evaluated for developing a child-friendly PZQ dosage form, with better product handling and biopharmaceutical properties, compared to MA materials. A 1:1 by wt PZQ-Povidone coground-was prepared in a vibrational mill under cryogenic conditions, for favoring amorphization. PZQ was neat ground to obtain its polymorphic form (Form B), which has an improved solubility and bioactivity. Then, activated PZQ powders were loaded into microparticles (MPs) by the SC technology, using the self-emulsifying agent Gelucire 50/13 as a carrier. Both, the activated powders and the corresponding loaded MPs were characterized for morphology, wettability, solubility, dissolution behavior, drug content, and drug solid state (Hot Stage Microscopy (HSM), Differential Scanning Calorimetry (DSC), X-Ray Powder Diffraction Studies (PXRD), and FT-IR). Samples were also in vitro tested for a comparison with PZQ against newly transformed schistosomula (NTS) and adults. MPs containing both MA systems showed a further increase of biopharmaceutical properties, compared to the milled powders, while maintaining PZQ bioactivity. MPs containing PZQ Form B represented the most promising product for designing a new PZQ formulation.

摘要

吡喹酮(PZQ)是治疗血吸虫感染的一线药物,被列入世界卫生组织儿童基本药物标准清单。在这项研究中,评估了机械化学活化(MA)和喷雾凝固(SC)技术的联合应用,以开发一种适合儿童的 PZQ 剂型,与 MA 材料相比,具有更好的产品处理和生物制药特性。在低温条件下,通过振动磨机以 1:1 重量比将 PZQ-聚乙烯吡咯烷酮共研磨,以促进非晶化。将 PZQ 进行纯研磨以获得其多晶型形式(形式 B),该形式具有提高的溶解度和生物活性。然后,通过 SC 技术将活化的 PZQ 粉末载入微颗粒(MPs)中,使用自乳化剂 Gelucire 50/13 作为载体。对活化粉末和相应负载的 MPs 进行了形态、润湿性、溶解度、溶解行为、药物含量和药物固体状态(热台显微镜(HSM)、差示扫描量热法(DSC)、X 射线粉末衍射研究(PXRD)和傅里叶变换红外光谱(FT-IR))的表征。还对样品进行了体外测试,以与 PZQ 对新转化的尾蚴(NTS)和成虫进行比较。与研磨粉末相比,含有 MA 系统的 MPs 进一步提高了生物制药特性,同时保持了 PZQ 的生物活性。含有 PZQ 形式 B 的 MPs 代表了设计新 PZQ 配方的最有前途的产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8704/6429213/1f8abe7041e3/ijms-20-01233-g001.jpg

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