研究了硫酸铜、福尔马林、高锰酸钾和敌百虫4种渔药对鲢(Hypophthalmichthys molitrix)鱼种的急性毒性。结果显示:硫酸铜的24 h LC50为7.71 mg/L,48 h LC50为6.11 mg/L,安全浓度为1.15 mg/L;福尔马林的24 hLC50为48.17 mg/L,48 h LC50为...研究了硫酸铜、福尔马林、高锰酸钾和敌百虫4种渔药对鲢(Hypophthalmichthys molitrix)鱼种的急性毒性。结果显示:硫酸铜的24 h LC50为7.71 mg/L,48 h LC50为6.11 mg/L,安全浓度为1.15 mg/L;福尔马林的24 hLC50为48.17 mg/L,48 h LC50为36.25 mg/L,安全浓度为6.16 mg/L;高锰酸钾的24 h LC50为3.87 mg/L,48 hLC50为2.75 mg/L,安全浓度为1.74 mg/L;敌百虫的24 h LC50为11.96 mg/L,48 h LC50为9.39 mg/L,安全浓度为0.42 mg/L。结果表明,敌百虫可安全使用,硫酸铜和福尔马林需慎用,高锰酸钾不适宜在鲢鱼种的防病中使用。展开更多
Micelles have been studied as drug delivery carriers for decades. Their use can potentially result in high drug accumulation at the target site through the enhanced permeability and retention effect. Nevertheless, the...Micelles have been studied as drug delivery carriers for decades. Their use can potentially result in high drug accumulation at the target site through the enhanced permeability and retention effect. Nevertheless, the lack of stability of micelles in the physiological environment limits their efficacy as a drug carrier. In particular, micelles tend to disassociate and prematurely release the encapsulated drugs, lowering delivery efficacy and creating toxicity concerns. Many efforts to enhance the stability of micelles have focused mainly on decreasing the critical micelle forming concentration and improving blood circulation. Herein, we review different strategies including crosslinking and non-crosslinking approaches designed to stabilize micelles and offer perspectives on future research directions.展开更多
文摘研究了硫酸铜、福尔马林、高锰酸钾和敌百虫4种渔药对鲢(Hypophthalmichthys molitrix)鱼种的急性毒性。结果显示:硫酸铜的24 h LC50为7.71 mg/L,48 h LC50为6.11 mg/L,安全浓度为1.15 mg/L;福尔马林的24 hLC50为48.17 mg/L,48 h LC50为36.25 mg/L,安全浓度为6.16 mg/L;高锰酸钾的24 h LC50为3.87 mg/L,48 hLC50为2.75 mg/L,安全浓度为1.74 mg/L;敌百虫的24 h LC50为11.96 mg/L,48 h LC50为9.39 mg/L,安全浓度为0.42 mg/L。结果表明,敌百虫可安全使用,硫酸铜和福尔马林需慎用,高锰酸钾不适宜在鲢鱼种的防病中使用。
基金This work was supported by the National Science Foundation （DMR-1410853） and National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health （DP2DK111910）.
文摘Micelles have been studied as drug delivery carriers for decades. Their use can potentially result in high drug accumulation at the target site through the enhanced permeability and retention effect. Nevertheless, the lack of stability of micelles in the physiological environment limits their efficacy as a drug carrier. In particular, micelles tend to disassociate and prematurely release the encapsulated drugs, lowering delivery efficacy and creating toxicity concerns. Many efforts to enhance the stability of micelles have focused mainly on decreasing the critical micelle forming concentration and improving blood circulation. Herein, we review different strategies including crosslinking and non-crosslinking approaches designed to stabilize micelles and offer perspectives on future research directions.
