多数小分子抗肿瘤药物水溶性差、循环半衰期短、生物利用度低，聚乙二醇修饰技术能够改善药物的药效学特性，是目前化学修饰的研究热点，具有很好的前景。阿霉素，是癌症化疗中经常使用的药物。不良反应包括脱发，骨髓抑制，恶心和呕吐，口腔粘膜炎等。PEG化阿霉素，能够提高生物活性的同时，降低其不良反应。PEG化药物的开发，需建立能够分析完整药物本身及释放药物的准确耐用的分析方法。但是，由于PEG化药物的分子量不唯一，直接分析挑战很大。由于缺少有效的方法，基于完整药物和释放药物水平的药代动力学研究很难进行。本课题拟通过建立分析PEG化药物和释放药物的CID In-Quadrupole的LC-Q/Q/Tof MS方法，进行阿霉素和PEG化阿霉素的比较药代动力学研究，就PEG化阿霉素，释放阿霉素、游离PEG进行系统性的研究，为PEG化阿霉素及PEG化纳米药物的开发及有效性评价提供分析工具和数据理论支撑。

Most of small molecule antitumor drugs have poor aqueous solubility, short circulation halftime and low bioavailability. PEGylation, covalent attaching polyethylene glycol (PEG) polymers to therapeutic compounds, is one of the most promising techniques to improve the biological efficacy of drugs. PEGylated molecules demonstrate enhanced solubility and stability. So far, many PEGylated drugs have been taken into clinical trials. Doxorubicin, sold under the trade names Adriamycin among others, is a medication used in cancer chemotherapy. Common adverse effects of doxorubicin include hair loss, myelosuppression , nausea and vomiting, oral mucositis and so on. PEGylation of doxorubicin could improve the biological efficacy and reduce the adverse effects of doxorubicin.The clinical development of PEGylated drugs requires accurate and robust methods for the qualitative and quantitative analysis of intact PEGylated molecules and the released compound in biological samples.However, owing to the heterogeneous nature of PEG, the mass of PEG or PEGylated molecules are uncertain, direct quantification of PEG or PEGylated drugs is challenging. Therefore, pharmacokinetic study of PEGylated drugs is very difficult due to the lack of effective analytical tools. In this study, we describe LC-Q/Q/Tof MS methods coupled with In-Quadrupole CID that can be utilized for the detection and measurement of PEGylated pharmaceuticals and the released compound in complex biological samples for comparative pharmacokinetic study of doxorubicin and PEG-doxorubicin. The method utilizing LC-MS/MS coupled with In-Quadrupole CID that is highly selective and sensitive to PEGylated compounds.PEGylated molecules undergo dissociation in the second Quadrupole of mass spectrometer to generate a series of high resolution. Via the LC-Q/Q/Tof MS methods coupled with In-Quadrupole CID, this research would study the Pharmacokinetic behavior of doxorubicin, mutiplescale PEG-doxorubicin, released PEG and their metabolites, also provides a powerful analysis tool and data theoretical support for the design and safety, effectiveness evalution of PEG-doxorubicin and PEGylated drugs.