Chiral Transport in Nanochannel Based Artificial Drug Transporters. Issue 6 (4th December 2022)
- Record Type:
- Journal Article
- Title:
- Chiral Transport in Nanochannel Based Artificial Drug Transporters. Issue 6 (4th December 2022)
- Main Title:
- Chiral Transport in Nanochannel Based Artificial Drug Transporters
- Authors:
- Yang, Lei
Sun, Zhongyue
Zhang, Siyun
Sun, Yue
Li, Haibing - Abstract:
- Abstract: The precise regulation of chiral drug transmembrane transport can be achieved through drug transporters in living organisms. However, implementing this process in vitro is still a formidable challenge due to the complexity of the biological systems that control drug enantiomeric transport. Herein, a facile and feasible strategy is employed to construct chiral L ‐tyrosine‐modified nanochannels ( L ‐Tyr nanochannels) based on polyethylene terephthalate film, which could enhance the chiral recognition of propranolol isomers ( R ‐/ S ‐PPL) for transmembrane transport. Moreover, conventional fluorescence spectroscopy, patch‐clamp technology, laser scanning confocal microscopy, and picoammeter technology are employed to evaluate the performance of nanochannels. The results show that the L ‐Tyr nanochannel have better chiral selectivity for R ‐/ S ‐PPL compared with the L ‐tryptophan ( L ‐Trp) channel, and the chiral selectivity coefficient is improved by about 4.21‐fold. Finally, a detailed theoretical analysis of the chirality selectivity mechanism is carried out. The findings would not only enrich the basic theory research related to chiral drug transmembrane transport, but also provide a new idea for constructing artificial channels to separate chiral drugs. Abstract : Herein, the L‐ amino acids are introduced through biomimetic strategy to fabricate the gated nanochannels for the chiral drugs. The gated transport effect of l ‐tyrosine nanochannels on propranololAbstract: The precise regulation of chiral drug transmembrane transport can be achieved through drug transporters in living organisms. However, implementing this process in vitro is still a formidable challenge due to the complexity of the biological systems that control drug enantiomeric transport. Herein, a facile and feasible strategy is employed to construct chiral L ‐tyrosine‐modified nanochannels ( L ‐Tyr nanochannels) based on polyethylene terephthalate film, which could enhance the chiral recognition of propranolol isomers ( R ‐/ S ‐PPL) for transmembrane transport. Moreover, conventional fluorescence spectroscopy, patch‐clamp technology, laser scanning confocal microscopy, and picoammeter technology are employed to evaluate the performance of nanochannels. The results show that the L ‐Tyr nanochannel have better chiral selectivity for R ‐/ S ‐PPL compared with the L ‐tryptophan ( L ‐Trp) channel, and the chiral selectivity coefficient is improved by about 4.21‐fold. Finally, a detailed theoretical analysis of the chirality selectivity mechanism is carried out. The findings would not only enrich the basic theory research related to chiral drug transmembrane transport, but also provide a new idea for constructing artificial channels to separate chiral drugs. Abstract : Herein, the L‐ amino acids are introduced through biomimetic strategy to fabricate the gated nanochannels for the chiral drugs. The gated transport effect of l ‐tyrosine nanochannels on propranolol enantiomers is found, which is not presented by other nanochannels. The research would provide a new idea for constructing artificial channels to regulate chiral drug delivery. … (more)
- Is Part Of:
- Small. Volume 19:Issue 6(2023)
- Journal:
- Small
- Issue:
- Volume 19:Issue 6(2023)
- Issue Display:
- Volume 19, Issue 6 (2023)
- Year:
- 2023
- Volume:
- 19
- Issue:
- 6
- Issue Sort Value:
- 2023-0019-0006-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-12-04
- Subjects:
- biomimetic nanochannels -- chirality -- drug transport -- gate effect -- propranolol
Nanotechnology -- Periodicals
Nanoparticles -- Periodicals
Microtechnology -- Periodicals
620.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1613-6829 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/smll.202205274 ↗
- Languages:
- English
- ISSNs:
- 1613-6810
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8309.952000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25732.xml