Electron beam(EB) degradation of perfluorooctanoic acid(PFOA) and perfluorooctane sulfonate(PFOS) in aqueous solutions was studied. It suggested that PFOA and PFOS degradation followed the pseudo-firstorder kinetics, ...Electron beam(EB) degradation of perfluorooctanoic acid(PFOA) and perfluorooctane sulfonate(PFOS) in aqueous solutions was studied. It suggested that PFOA and PFOS degradation followed the pseudo-firstorder kinetics, and degradation rates increased with increasing initial p H. Radical scavengers' experiments indicated that hydrated electron and hydrogen radical were important in the electron beam degradation of PFOA and PFOS, especially hydrated electron. The decomposition efficiencies were 95.7% for PFOA and 85.9% for PFOS, by EB irradiation in an anoxic alkaline solution(p H = 13).The potential degradation pathways of PFOA and PFOS by electron beam irradiation through defluorination and the removal of CH_2 unit were proposed.展开更多
Oligonucleotide therapeutics have great potential to target the currently undruggable genes and to generate entirely new therapeutic paradigms in multiple types of disease,thus having attracted much attention in recen...Oligonucleotide therapeutics have great potential to target the currently undruggable genes and to generate entirely new therapeutic paradigms in multiple types of disease,thus having attracted much attention in recent years.However,their applications are greatly hindered by a lack of safe and efficient oligonucleotide-delivery vectors.Polyplex nanovesicles formed from oligonucleotides and the cationic block have shown exceptional features for the delivery of therapeutic oligonucleotides and other biopharmaceuticals.Nevertheless,these polyplex nanovesicles are deeply fraught with difficulty in tolerating physiological ionic strength.Inspired by the high binding ability between the dipicolylamine(DPA)/zinc(Ⅱ)complex and the phosphodiester moieties of oligonucleotides,herein,we designed a coordinative cationic block to solve the intrinsic stability dilemma.Moreover,we found the stability of the resulted polyplex nanovesicles could be easily tuned by the content of coordinated zinc ions.In vitro cellular studies implied that the prepared zinc(Ⅱ)-coordinative polyplex nanovesicles preferred to retain in the lysosomes upon internalization,making them ideal delivery candidates for the lysosome-targeting oligonucleotide therapeutics.展开更多
基金supported by the National Natural Science Foundation of China(Nos.11675098,41430644,41473090,41373098)Program for Changjiang Scholars and Innovative Research Team in University(No.IRT13078)
文摘Electron beam(EB) degradation of perfluorooctanoic acid(PFOA) and perfluorooctane sulfonate(PFOS) in aqueous solutions was studied. It suggested that PFOA and PFOS degradation followed the pseudo-firstorder kinetics, and degradation rates increased with increasing initial p H. Radical scavengers' experiments indicated that hydrated electron and hydrogen radical were important in the electron beam degradation of PFOA and PFOS, especially hydrated electron. The decomposition efficiencies were 95.7% for PFOA and 85.9% for PFOS, by EB irradiation in an anoxic alkaline solution(p H = 13).The potential degradation pathways of PFOA and PFOS by electron beam irradiation through defluorination and the removal of CH_2 unit were proposed.
基金financially supported by the National Key Research and Development Program of China (No.2021YFA1201200)the National Natural Science Foundation of China (Nos. 51833008, 52173141 and 82102192)+1 种基金Zhejiang Provincial Key Research and Development Program (No.2020C01123)China Postdoctoral Science Foundation (No.2019M662059)
文摘Oligonucleotide therapeutics have great potential to target the currently undruggable genes and to generate entirely new therapeutic paradigms in multiple types of disease,thus having attracted much attention in recent years.However,their applications are greatly hindered by a lack of safe and efficient oligonucleotide-delivery vectors.Polyplex nanovesicles formed from oligonucleotides and the cationic block have shown exceptional features for the delivery of therapeutic oligonucleotides and other biopharmaceuticals.Nevertheless,these polyplex nanovesicles are deeply fraught with difficulty in tolerating physiological ionic strength.Inspired by the high binding ability between the dipicolylamine(DPA)/zinc(Ⅱ)complex and the phosphodiester moieties of oligonucleotides,herein,we designed a coordinative cationic block to solve the intrinsic stability dilemma.Moreover,we found the stability of the resulted polyplex nanovesicles could be easily tuned by the content of coordinated zinc ions.In vitro cellular studies implied that the prepared zinc(Ⅱ)-coordinative polyplex nanovesicles preferred to retain in the lysosomes upon internalization,making them ideal delivery candidates for the lysosome-targeting oligonucleotide therapeutics.
