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LC-MS/MS 法同时测定阿霉素和黄芩素的含量:制剂及药代动力学应用。

LC-MS/MS method for simultaneous Doxorubicin and Baicalein estimation: formulation and pharmacokinetic applications.

机构信息

Division of Pharmaceutics & Pharmacokinetics, CSIR-Central Drug Research Institute, Lucknow, 226031, India.

Academy of Scientific & Innovative Research (AcSIR), Ghaziabad, 201002, India.

出版信息

Nanomedicine (Lond). 2024;19(25):2085-2097. doi: 10.1080/17435889.2024.2390348. Epub 2024 Sep 3.

Abstract

Combinatorial delivery of Doxorubicin (DOX) and Baicalein (BAC) has a potential to improve breast cancer treatment by mitigating the cardiotoxicity induced by DOX. The nanoformulation has been optimized and subjected to pharmacokinetic studies using LC-MS/MS. Nanoformulation bearing DOX and BAC was optimized using quality by design approach and method validation was done following USFDA guidelines. The particle size, PDI and zeta potential of developed nanoformulation were 162.56 ± 2.21 nm, 0.102 ± 0.03 and -16.5 ± 1.21 mV, respectively. DOX-BAC-SNEDDs had a higher AUC values of 6128.84 ± 68.71 and 5896.62 ± 99.31 ng/mL/h as compared with DOX-BAC suspension. These findings hold promise for advancing breast cancer treatment and facilitating therapeutic drug monitoring.

摘要

多柔比星(DOX)和黄芩素(BAC)联合递药有潜力通过减轻 DOX 引起的心脏毒性来改善乳腺癌的治疗效果。该纳米制剂已经过优化,并使用 LC-MS/MS 进行了药代动力学研究。采用质量设计方法对载 DOX 和 BAC 的纳米制剂进行了优化,并按照美国 FDA 指南进行了方法验证。所开发的纳米制剂的粒径、PDI 和 Zeta 电位分别为 162.56±2.21nm、0.102±0.03 和-16.5±1.21mV。与 DOX-BAC 混悬剂相比,DOX-BAC-SNEDDs 的 AUC 值分别提高了 6128.84±68.71 和 5896.62±99.31ng/mL/h。这些发现为推进乳腺癌治疗和促进治疗药物监测提供了希望。

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