Daniel A. Paterson, Aggie Lawer, Jared Davidson, Sarah Hook and Allan B. Gamble
{"title":"硫化氢生成的刺激响应型硫代氨基甲酸酯基聚合物颗粒†","authors":"Daniel A. Paterson, Aggie Lawer, Jared Davidson, Sarah Hook and Allan B. Gamble","doi":"10.1039/D5LP00040H","DOIUrl":null,"url":null,"abstract":"<p >Hydrogen sulfide (H<small><sub>2</sub></small>S) imbalance has been implicated in pathologies, and reinstating H<small><sub>2</sub></small>S homeostasis could be a useful therapeutic strategy. However, delivery of H<small><sub>2</sub></small>S to the disease site remains a challenge. Functionalised nanoformulations could be used as a strategy to deliver high concentrations of H<small><sub>2</sub></small>S in a targeted manner. Use of a disease-associated trigger that activates and releases H<small><sub>2</sub></small>S would provide therapeutic selectivity. As proof-of-concept, synthesis and formulation of block co-polymers bearing a thiocarbamate bond, a carbonyl sulfide (COS) precursor, is described. Activation by hydrogen peroxide (H<small><sub>2</sub></small>O<small><sub>2</sub></small>), and a subsequent 1,6-self-immolation process leads to release of COS, which in the presence of carbonic anhydrase is hydrolysed to H<small><sub>2</sub></small>S. H<small><sub>2</sub></small>S generation was exemplified by reduction of an azido-pro-fluorophore. Formulation of the polymer resulted in compound vesicles that were able to encapsulate a model drug and could be useful in future biological studies exploring delivery of H<small><sub>2</sub></small>S as a therapeutic, or to activate azido-masked prodrug/pro-fluorophore in areas of high reactive oxygen species (ROS).</p>","PeriodicalId":101139,"journal":{"name":"RSC Applied Polymers","volume":" 4","pages":" 926-933"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/lp/d5lp00040h?page=search","citationCount":"0","resultStr":"{\"title\":\"Stimuli-responsive thiocarbamate-based polymeric particles for hydrogen sulfide generation†\",\"authors\":\"Daniel A. Paterson, Aggie Lawer, Jared Davidson, Sarah Hook and Allan B. Gamble\",\"doi\":\"10.1039/D5LP00040H\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Hydrogen sulfide (H<small><sub>2</sub></small>S) imbalance has been implicated in pathologies, and reinstating H<small><sub>2</sub></small>S homeostasis could be a useful therapeutic strategy. However, delivery of H<small><sub>2</sub></small>S to the disease site remains a challenge. Functionalised nanoformulations could be used as a strategy to deliver high concentrations of H<small><sub>2</sub></small>S in a targeted manner. Use of a disease-associated trigger that activates and releases H<small><sub>2</sub></small>S would provide therapeutic selectivity. As proof-of-concept, synthesis and formulation of block co-polymers bearing a thiocarbamate bond, a carbonyl sulfide (COS) precursor, is described. Activation by hydrogen peroxide (H<small><sub>2</sub></small>O<small><sub>2</sub></small>), and a subsequent 1,6-self-immolation process leads to release of COS, which in the presence of carbonic anhydrase is hydrolysed to H<small><sub>2</sub></small>S. H<small><sub>2</sub></small>S generation was exemplified by reduction of an azido-pro-fluorophore. Formulation of the polymer resulted in compound vesicles that were able to encapsulate a model drug and could be useful in future biological studies exploring delivery of H<small><sub>2</sub></small>S as a therapeutic, or to activate azido-masked prodrug/pro-fluorophore in areas of high reactive oxygen species (ROS).</p>\",\"PeriodicalId\":101139,\"journal\":{\"name\":\"RSC Applied Polymers\",\"volume\":\" 4\",\"pages\":\" 926-933\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-05-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/lp/d5lp00040h?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Applied Polymers\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/lp/d5lp00040h\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Applied Polymers","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/lp/d5lp00040h","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Stimuli-responsive thiocarbamate-based polymeric particles for hydrogen sulfide generation†
Hydrogen sulfide (H2S) imbalance has been implicated in pathologies, and reinstating H2S homeostasis could be a useful therapeutic strategy. However, delivery of H2S to the disease site remains a challenge. Functionalised nanoformulations could be used as a strategy to deliver high concentrations of H2S in a targeted manner. Use of a disease-associated trigger that activates and releases H2S would provide therapeutic selectivity. As proof-of-concept, synthesis and formulation of block co-polymers bearing a thiocarbamate bond, a carbonyl sulfide (COS) precursor, is described. Activation by hydrogen peroxide (H2O2), and a subsequent 1,6-self-immolation process leads to release of COS, which in the presence of carbonic anhydrase is hydrolysed to H2S. H2S generation was exemplified by reduction of an azido-pro-fluorophore. Formulation of the polymer resulted in compound vesicles that were able to encapsulate a model drug and could be useful in future biological studies exploring delivery of H2S as a therapeutic, or to activate azido-masked prodrug/pro-fluorophore in areas of high reactive oxygen species (ROS).