Synthesis and NMR characterization of PEGylated β-cyclodextrins

Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial applications. We have carried out the synthesis of PEGylated β-CDs through ether chemical bond linkage between β-CD and poly(ethylene glycol...

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Published inJournal of inclusion phenomena and macrocyclic chemistry Vol. 103; no. 5-6; pp. 213 - 222
Main Authors Nguyen, Kim Trang Huu, Ba, Yong
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.06.2023
Springer Nature B.V
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Abstract Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial applications. We have carried out the synthesis of PEGylated β-CDs through ether chemical bond linkage between β-CD and poly(ethylene glycol) methyl ether (MPEG). The combination of β-CD with poly(ethylene glycol) will benefit from PEG’s properties including high water solubility, nontoxicity, non-immunogenicity, biocompatibility, and biodegradability. The synthesis proceeded through three steps: (a) tosylation of MPEG; (b) deprotonation of hydroxyl groups of β-CD using NaH; and (c) the combination of the above two intermediates through the S N 2 mechanism to obtain the MPEG-β-CD compounds. The products were confirmed by MALDI-TOF mass spectrometry, and their structures were analyzed using 1 H 2D COSY and ROESY NMR methods. It was found that the site of PEGylation occurred on the (OH)6 site of β-CD. The inclusion property of the MPEG-β-CDs was demonstrated by forming inclusion complexes with 1-fluroroadamantane. We anticipate that the newly added properties of the MPEG to β-CD promote their pharmaceutical and other industrial applications.
AbstractList Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial applications. We have carried out the synthesis of PEGylated β-CDs through ether chemical bond linkage between β-CD and poly(ethylene glycol) methyl ether (MPEG). The combination of β-CD with poly(ethylene glycol) will benefit from PEG’s properties including high water solubility, nontoxicity, non-immunogenicity, biocompatibility, and biodegradability. The synthesis proceeded through three steps: (a) tosylation of MPEG; (b) deprotonation of hydroxyl groups of β-CD using NaH; and (c) the combination of the above two intermediates through the S N 2 mechanism to obtain the MPEG-β-CD compounds. The products were confirmed by MALDI-TOF mass spectrometry, and their structures were analyzed using 1 H 2D COSY and ROESY NMR methods. It was found that the site of PEGylation occurred on the (OH)6 site of β-CD. The inclusion property of the MPEG-β-CDs was demonstrated by forming inclusion complexes with 1-fluroroadamantane. We anticipate that the newly added properties of the MPEG to β-CD promote their pharmaceutical and other industrial applications.
Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial applications. We have carried out the synthesis of PEGylated β-CDs through ether chemical bond linkage between β-CD and poly(ethylene glycol) methyl ether (MPEG). The combination of β-CD with poly(ethylene glycol) will benefit from PEG’s properties including high water solubility, nontoxicity, non-immunogenicity, biocompatibility, and biodegradability. The synthesis proceeded through three steps: (a) tosylation of MPEG; (b) deprotonation of hydroxyl groups of β-CD using NaH; and (c) the combination of the above two intermediates through the SN2 mechanism to obtain the MPEG-β-CD compounds. The products were confirmed by MALDI-TOF mass spectrometry, and their structures were analyzed using 1H 2D COSY and ROESY NMR methods. It was found that the site of PEGylation occurred on the (OH)6 site of β-CD. The inclusion property of the MPEG-β-CDs was demonstrated by forming inclusion complexes with 1-fluroroadamantane. We anticipate that the newly added properties of the MPEG to β-CD promote their pharmaceutical and other industrial applications.
Author Nguyen, Kim Trang Huu
Ba, Yong
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Keywords Water solubility
PEGylation
2D NMR
β-cyclodextrin
Inclusion complex
Poly(ethylene glycol)
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Snippet Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial...
Cyclodextrins (CDs) and their chemical derivatives are well-known as effective carriers for low-water-soluble molecules for pharmaceutical and other industrial...
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SubjectTerms Biocompatibility
Chemical bonds
Chemical synthesis
Chemistry
Chemistry and Materials Science
Crystallography and Scattering Methods
Cyclodextrins
Food Science
Hydroxyl groups
Inclusion complexes
Industrial applications
Mass spectrometry
MPEG encoders
NMR
Nuclear magnetic resonance
Organic Chemistry
Original Article
Pharmaceuticals
Polyethylene glycol
Two dimensional analysis
Title Synthesis and NMR characterization of PEGylated β-cyclodextrins
URI https://link.springer.com/article/10.1007/s10847-023-01188-z
https://www.proquest.com/docview/2829206402
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