Literature DB >> 70229

Monosialoganglioside liposome-entrapped enzyme uptake by hepatic cells.

A Surolia, B K Bachhawat.   

Abstract

Monosialoganglioside liposomes are rapidly taken up by the liver as compared to dicetylphosphate, phosphatidic acid or neutral liposomes. Asialoganglioside GM 1 liposomes are taken up with the same avidity as ganglioside GM 1 liposomes. Competition experiments with asialofetuin suggest that this uptake is mediated by specific recognition of the terminal galactose residues of the glyco-lipid liposomes by the receptor present on the plasma membrane of the parenchymal cells of liver. Thus liposomes containing glycolipids with terminal beta-galactosyl residues should provide an approach for specifically directing biologically active molecules to liver parenchymal cells.

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Year:  1977        PMID: 70229     DOI: 10.1016/0304-4165(77)90296-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  3 in total

1.  Synthesis of neoglycopeptides and analyses of their biodistribution in vivo to identify tissue specific uptake and novel putative membrane lectins.

Authors:  D Gupta; A Surolia
Journal:  Glycoconj J       Date:  1994-12       Impact factor: 2.916

2.  Plant glycosides in a liposomal drug-delivery system.

Authors:  N Das; B K Bachhawat; S B Mahato; M K Basu
Journal:  Biochem J       Date:  1987-10-15       Impact factor: 3.857

3.  Stealth properties to improve therapeutic efficacy of drug nanocarriers.

Authors:  Stefano Salmaso; Paolo Caliceti
Journal:  J Drug Deliv       Date:  2013-03-07
  3 in total

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