通过pH敏感腙键共轭mPEG-b-PCL共聚物的阿霉素量的测定

Gülhan Işik, A. Tezcaner, N. Hasirci, A. Kiziltay
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引用次数: 0

摘要

目的:寻找抗肿瘤药物多柔比星(DOX)与甲氧基聚乙二醇嵌段聚己内酯(mPEG-b-PCL)通过pH敏感腙键结合的有效介质,并测定结合药物的量。方法:在两种不同的介质[二甲亚砜(DMSO)和甲醇-三氟乙酸(MeOH-TFA)]中进行DOX偶联。采用两种不同的方法测定结合药物的用量。一种方法是在氯仿:甲醇(Ch: MeOH, 1:1 v/v)溶液中溶解共轭物,不考虑pH响应性;另一种方法是在酸性介质中破坏pH敏感的腙键[使用0.1 M盐酸(HCl)、浓盐酸(12 M HCl)和浓硫酸(18.3 M H2SO4)三种不同的介质]。结果:在MeOH-TFA溶液中偶联和浓硫酸处理后的聚合物-药物偶联物的偶联效率最高。迅速被免疫系统识别(12)。另一方面,聚乙二醇是亲水的,可以从免疫系统中逃脱。科学家们制备或使用PEG和PCL的共聚物或三嵌段聚合物,并制备纳米颗粒或胶束作为药物传递载体,并评估其体外和体内性能(13)。Gong等研究了PEG-PCL-PEG胶束的亲和力(14)。Hu等人用PCL-PEG-PCL聚合物制备胶束和聚合体作为药物载体(15)。Chen等人对功能化聚乙二醇制备的负载多柔比星的PEG-PCL胶束的细胞毒性进行了评估,并报道了有希望的结果(16)。准确测定药物偶联是很重要的,因为给病人高剂量可能会产生一些不想要的症状,如心肌病。结论:本文认为,MeOH-TFA法是测定DOX与M - tfa偶联的较好方法,M - tfa法是测定DOX通过聚合物偶联量的较好方法
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Determination of doxorubicin amount conjugated to mPEG-b-PCL copolymer via pH sensitive hydrazone bond
Objective: The aim of this study was to find the efficient medium to bind an anticancer drug, Doxorubicin (DOX), to a synthesized polymer, methoxy poly(ethylene glycol)-block-polycaprolactone (mPEG-b-PCL) via pH sensitive hydrazone bonds and to determine the amount of conjugated drug. Methods: DOX conjugation was carried out in two different media [dimethyl sulfoxide (DMSO) and methanol-trifluoroacetic acid (MeOH-TFA)]. The amount of conjugated drug was determined with two different methods. One method was applied the dissolution of the conjugate in chloroform: methanol (Ch: MeOH, 1: 1 v/v) solution without considering pH responsiveness, and the other method was after breaking pH sensitive hydrazone bonds in acidic medium [using three different media as 0.1 M hydrochloric acid (HCl), concentrated HCl (12 M HCl) and concentrated sulfuric acid (18.3 M H2SO4)]. Results: The highest conjugation efficiency was obtained when the conjugation was achieved in MeOH-TFA solution, and for the polymer-drug conjugates after the treatment with concentrated sulfuric acid. recognized by immune system rapidly (12). On the other hand, PEG is hydrophilic and can escape from the immune system. Scientists prepared or used copolymers or tri-block-polymers of PEG and PCL and prepared either nanoparticles or micelles as drug delivery vehicles and evaluated in vitro and in vivo properties (13). Gong et al studied affinity of PEG-PCL-PEG micelles (14). Hu et al prepared micelles and polymersomes from PCL-PEG-PCL polymers to be used as drug carriers (15). Cytotoxic properties of Doxorubicin loaded PEG-PCL micelles prepared with functionalized PEGs were evaluated by Chen et al. and promising results were reported (16). An accurate determination of drug conjugation is important since higher dose given to a patient may create some unwanted symptoms like cardiomyopathy. In this study, methoxy konjugasyonu Conclusion: It was concluded that, MeOH-TFA method was a good method for conjugation of DOX to M) method was better other present in literature for determination of the amount of DOX linked to the polymer via
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