Overlook of chiral consideration in transdermal drug delivery increases administrated dose and risk of side effects,decreasing therapeutical effects.To improve the transdermal delivery efficiency of eutomer,this work ...Overlook of chiral consideration in transdermal drug delivery increases administrated dose and risk of side effects,decreasing therapeutical effects.To improve the transdermal delivery efficiency of eutomer,this work focused on investigating the law and mechanism of enantioselective enhancing effects of chiral permeation enhancers on drug enantiomers.Chiral nonsteroidal anti-inflammatory drugs and terpene permeation enhancers were selected as model drug and enhancers.The results indicated that the L-isomer of permeation enhancers increased the skin absorption of S-enantiomer of drug and D-isomer improve the permeation of R-enantiomer,in which the enhancement effect(ER)of Lmenthol on S-enantiomer(ER=3.23)was higher than that on R-enantiomer(ER=1.49).According to the pharmacokinetics results,L-menthol tended to enhance the permeation of S-enantiomer better than R-enantiomer(2.56 fold),and showed excellent in vitro/in vivo correlations.The mechanism study showed that L-isomer of permeation enhancers improved the permeation of S-enantiomer by increasing the retention,but the D-isomer by improving partition for better permeation.Enantioselective mechanism indicated that the weaker chiral H-bond interaction between drug-chiral enhancers was caused by the enantiomeric conformation.Additionally,stronger chiral enhancers-skin interaction between L-isomer and S-conformation of ceramide produced better enhancing effects.In conclusion,enantioselective interaction of chiral drug-chiral enhancers and chiral enhancers-chiral skin played a critical role in transdermal drug delivery,rational utilization of which contributed to improving the uptake of eutomer and inhibiting distomers to decrease a half of dose and side effects,increasing transdermal therapeutical efficiency.展开更多
Amino acid homochirality, as a unique behavior of life, could have originated synchronously with the genetic code. In this paper, phosphoryl amino-acid -5′-nucleosides with P-N bond are postulated to be a chiral orig...Amino acid homochirality, as a unique behavior of life, could have originated synchronously with the genetic code. In this paper, phosphoryl amino-acid -5′-nucleosides with P-N bond are postulated to be a chiral origin model in prebiotic molecular evolution. The enthalpy change in the intramolecular interaction between the nucleotide base and the amino-acid side-chain determines the sta-bility of the particular complex, resulting in a preferred conformation associated with the chirality of amino acids. Based on the theoretical model, our experiments and calculations show that the chiral selection of the earliest amino acids for L-enantiomers seems to be a strict stereochemi-cal/physicochemical determinism. As other amino acids developed biosynthetically from the earliest amino acids, we infer that the chirality of the later amino acids was inherited from the precursor amino acids. This idea probably goes far back in history, but it is hoped that it will be a guide for further ex-periments in this area.展开更多
基金supported by the National Natural Science Foundation of China(Grant No.82273879)
文摘Overlook of chiral consideration in transdermal drug delivery increases administrated dose and risk of side effects,decreasing therapeutical effects.To improve the transdermal delivery efficiency of eutomer,this work focused on investigating the law and mechanism of enantioselective enhancing effects of chiral permeation enhancers on drug enantiomers.Chiral nonsteroidal anti-inflammatory drugs and terpene permeation enhancers were selected as model drug and enhancers.The results indicated that the L-isomer of permeation enhancers increased the skin absorption of S-enantiomer of drug and D-isomer improve the permeation of R-enantiomer,in which the enhancement effect(ER)of Lmenthol on S-enantiomer(ER=3.23)was higher than that on R-enantiomer(ER=1.49).According to the pharmacokinetics results,L-menthol tended to enhance the permeation of S-enantiomer better than R-enantiomer(2.56 fold),and showed excellent in vitro/in vivo correlations.The mechanism study showed that L-isomer of permeation enhancers improved the permeation of S-enantiomer by increasing the retention,but the D-isomer by improving partition for better permeation.Enantioselective mechanism indicated that the weaker chiral H-bond interaction between drug-chiral enhancers was caused by the enantiomeric conformation.Additionally,stronger chiral enhancers-skin interaction between L-isomer and S-conformation of ceramide produced better enhancing effects.In conclusion,enantioselective interaction of chiral drug-chiral enhancers and chiral enhancers-chiral skin played a critical role in transdermal drug delivery,rational utilization of which contributed to improving the uptake of eutomer and inhibiting distomers to decrease a half of dose and side effects,increasing transdermal therapeutical efficiency.
基金Supported by the National Natural Science Foundation of China (Grant No. 20572061)the Science Foundation of Xiamen University (Grant No. Z03120)
文摘Amino acid homochirality, as a unique behavior of life, could have originated synchronously with the genetic code. In this paper, phosphoryl amino-acid -5′-nucleosides with P-N bond are postulated to be a chiral origin model in prebiotic molecular evolution. The enthalpy change in the intramolecular interaction between the nucleotide base and the amino-acid side-chain determines the sta-bility of the particular complex, resulting in a preferred conformation associated with the chirality of amino acids. Based on the theoretical model, our experiments and calculations show that the chiral selection of the earliest amino acids for L-enantiomers seems to be a strict stereochemi-cal/physicochemical determinism. As other amino acids developed biosynthetically from the earliest amino acids, we infer that the chirality of the later amino acids was inherited from the precursor amino acids. This idea probably goes far back in history, but it is hoped that it will be a guide for further ex-periments in this area.
