Ling-Mei Li, Yi-Pin Xie, Yu-Rong Qin, Hai-Ping Chu, Hui Xie, De-Jin Zang, Teng Liu
{"title":"治疗癌症和克服 MDR 的肿瘤微环境响应型药物自我递送系统","authors":"Ling-Mei Li, Yi-Pin Xie, Yu-Rong Qin, Hai-Ping Chu, Hui Xie, De-Jin Zang, Teng Liu","doi":"10.1007/s12598-024-02892-6","DOIUrl":null,"url":null,"abstract":"<div><p>Tumor microenvironment-responsive drug self-delivery systems utilize tumor microenvironment-responsive chemical bonds to link anti-tumor drugs, exploiting the hydrophilic and hydrophobic properties of different drugs to form amphiphilic prodrug molecules with self-assembly characteristics. Upon stimulation by specific factors in the tumor microenvironment, these amphiphilic prodrug molecules can release drugs at precise sites within the tumor. These strategies significantly increase the drug concentration at the tumor site while effectively reducing the damage of anti-cancer drugs to normal tissues. Owing to the advanced delivery strategies such as synergistic administration and controlled drug release, tumor microenvironment-responsive drug self-delivery systems hold great potential for treating malignant tumors with multidrug resistance (MDR). At the same time, the stimulus-reactivity of metal complexes provides an important opportunity to design site-specific prodrugs that can maximize therapeutic efficacy while minimizing adverse side effects of metal drugs. This innovative drug design complements the tumor microenvironment-responsive self-delivery system, providing more feasible therapeutic strategies and possibilities in the field of cancer therapy and drug delivery. This work provides a comprehensive review of recent advancements in drug self-delivery systems, offering insights into their potential applications in cancer therapy and MDR reversal.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":749,"journal":{"name":"Rare Metals","volume":"44 1","pages":"1 - 33"},"PeriodicalIF":9.6000,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tumor microenvironment-responsive drug self-delivery systems to treat cancer and overcome MDR\",\"authors\":\"Ling-Mei Li, Yi-Pin Xie, Yu-Rong Qin, Hai-Ping Chu, Hui Xie, De-Jin Zang, Teng Liu\",\"doi\":\"10.1007/s12598-024-02892-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Tumor microenvironment-responsive drug self-delivery systems utilize tumor microenvironment-responsive chemical bonds to link anti-tumor drugs, exploiting the hydrophilic and hydrophobic properties of different drugs to form amphiphilic prodrug molecules with self-assembly characteristics. Upon stimulation by specific factors in the tumor microenvironment, these amphiphilic prodrug molecules can release drugs at precise sites within the tumor. These strategies significantly increase the drug concentration at the tumor site while effectively reducing the damage of anti-cancer drugs to normal tissues. Owing to the advanced delivery strategies such as synergistic administration and controlled drug release, tumor microenvironment-responsive drug self-delivery systems hold great potential for treating malignant tumors with multidrug resistance (MDR). At the same time, the stimulus-reactivity of metal complexes provides an important opportunity to design site-specific prodrugs that can maximize therapeutic efficacy while minimizing adverse side effects of metal drugs. This innovative drug design complements the tumor microenvironment-responsive self-delivery system, providing more feasible therapeutic strategies and possibilities in the field of cancer therapy and drug delivery. This work provides a comprehensive review of recent advancements in drug self-delivery systems, offering insights into their potential applications in cancer therapy and MDR reversal.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":749,\"journal\":{\"name\":\"Rare Metals\",\"volume\":\"44 1\",\"pages\":\"1 - 33\"},\"PeriodicalIF\":9.6000,\"publicationDate\":\"2024-08-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rare Metals\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12598-024-02892-6\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare Metals","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s12598-024-02892-6","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Tumor microenvironment-responsive drug self-delivery systems to treat cancer and overcome MDR
Tumor microenvironment-responsive drug self-delivery systems utilize tumor microenvironment-responsive chemical bonds to link anti-tumor drugs, exploiting the hydrophilic and hydrophobic properties of different drugs to form amphiphilic prodrug molecules with self-assembly characteristics. Upon stimulation by specific factors in the tumor microenvironment, these amphiphilic prodrug molecules can release drugs at precise sites within the tumor. These strategies significantly increase the drug concentration at the tumor site while effectively reducing the damage of anti-cancer drugs to normal tissues. Owing to the advanced delivery strategies such as synergistic administration and controlled drug release, tumor microenvironment-responsive drug self-delivery systems hold great potential for treating malignant tumors with multidrug resistance (MDR). At the same time, the stimulus-reactivity of metal complexes provides an important opportunity to design site-specific prodrugs that can maximize therapeutic efficacy while minimizing adverse side effects of metal drugs. This innovative drug design complements the tumor microenvironment-responsive self-delivery system, providing more feasible therapeutic strategies and possibilities in the field of cancer therapy and drug delivery. This work provides a comprehensive review of recent advancements in drug self-delivery systems, offering insights into their potential applications in cancer therapy and MDR reversal.
期刊介绍:
Rare Metals is a monthly peer-reviewed journal published by the Nonferrous Metals Society of China. It serves as a platform for engineers and scientists to communicate and disseminate original research articles in the field of rare metals. The journal focuses on a wide range of topics including metallurgy, processing, and determination of rare metals. Additionally, it showcases the application of rare metals in advanced materials such as superconductors, semiconductors, composites, and ceramics.