Self‐Assembly and Transport Behaviour of Non‐ionic Fluorinated and Alkylated Amphiphiles for Drug Delivery. Issue 35 (16th September 2022)
- Record Type:
- Journal Article
- Title:
- Self‐Assembly and Transport Behaviour of Non‐ionic Fluorinated and Alkylated Amphiphiles for Drug Delivery. Issue 35 (16th September 2022)
- Main Title:
- Self‐Assembly and Transport Behaviour of Non‐ionic Fluorinated and Alkylated Amphiphiles for Drug Delivery
- Authors:
- Kumar, Anoop
Krishna,
Sharma, Antara
Dhankhar, Jyoti
Syeda, Saima
Shrivastava, Anju
Sharma, Sunil K. - Abstract:
- Abstract: A newer series of AB2 typed non‐ionic amphiphiles have been synthesized using p ‐hydroxybenzoate as a central core, which is further functionalized with two hydrophilic units, i. e. D‐lactose/poly(glycerol) dendron [G2.0]/monomethoxy poly(ethyleneglycol) and a hydrophobic alkyl/fluoroalkyl moiety. The aggregation behaviour of the synthesised amphiphiles in aqueous medium was studied using fluorescence spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM) and were found to form nano‐sized aggregates. The potential of these amphiphiles to act as nanocarrier was studied using model hydrophobic probe Nile red and nimodipine by recording their UV‐visible and fluorescence spectroscopic data. For comparison purpose, analogous AB type amphiphiles were also synthesized and their transport ability analysed. A study of cell viability in HeLa cells revealed that all synthesized amphiphiles are well tolerated at the concentrations studied. The immobilized hydrolase Novozym‐435 was used to release the encapsulated dye from the inner hydrophobic core of micellar structures of synthesized amphiphiles in vitro. Abstract : A newer series of non‐ionic amphiphiles have been synthesized by using p ‐hydroxybenzoate as a central core, which is further functionalized with different hydrophilic and hydrophobic units. The model hydrophobic guests were used to examine the transport and enzyme triggered release potential of nano‐sized aggregates formed byAbstract: A newer series of AB2 typed non‐ionic amphiphiles have been synthesized using p ‐hydroxybenzoate as a central core, which is further functionalized with two hydrophilic units, i. e. D‐lactose/poly(glycerol) dendron [G2.0]/monomethoxy poly(ethyleneglycol) and a hydrophobic alkyl/fluoroalkyl moiety. The aggregation behaviour of the synthesised amphiphiles in aqueous medium was studied using fluorescence spectroscopy, dynamic light scattering (DLS) and transmission electron microscopy (TEM) and were found to form nano‐sized aggregates. The potential of these amphiphiles to act as nanocarrier was studied using model hydrophobic probe Nile red and nimodipine by recording their UV‐visible and fluorescence spectroscopic data. For comparison purpose, analogous AB type amphiphiles were also synthesized and their transport ability analysed. A study of cell viability in HeLa cells revealed that all synthesized amphiphiles are well tolerated at the concentrations studied. The immobilized hydrolase Novozym‐435 was used to release the encapsulated dye from the inner hydrophobic core of micellar structures of synthesized amphiphiles in vitro. Abstract : A newer series of non‐ionic amphiphiles have been synthesized by using p ‐hydroxybenzoate as a central core, which is further functionalized with different hydrophilic and hydrophobic units. The model hydrophobic guests were used to examine the transport and enzyme triggered release potential of nano‐sized aggregates formed by these amphiphiles in aqueous media. … (more)
- Is Part Of:
- ChemistrySelect. Volume 7:Issue 35(2022)
- Journal:
- ChemistrySelect
- Issue:
- Volume 7:Issue 35(2022)
- Issue Display:
- Volume 7, Issue 35 (2022)
- Year:
- 2022
- Volume:
- 7
- Issue:
- 35
- Issue Sort Value:
- 2022-0007-0035-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-09-16
- Subjects:
- Amphiphiles -- Cytotoxicity -- Drug delivery -- Encapsulation -- Self-assembly
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.202203274 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23913.xml