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Investigations on Alternate Approach to Target Mannose Receptors on Macrophages using 4-Sulfated N-Acetyl Galactosamine more Efficiently as Compared to Mannose Decorated Liposomes: an Application in Drug Delivery

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Singodia, Deepak
Verma, Ashwni
Verma, R K
Mishra, P R
 
Date 2012-07-27T07:14:45Z
2012-07-27T07:14:45Z
2012
 
Identifier Nanomedicine: Nanotechnology, Biology and Medicine 2012 8(4), 468–477
http://hdl.handle.net/123456789/837
 
Description In the present study the targeting potential of two different ligands i.e palmitoyl mannose (Man-Lip) and 4-SO4GalNAc (Sulf-Lip) to resident macrophages have been investigated after having decorated on the surface of Amphotericin B (AmB) loaded liposomes. In case of Sulf-Lip, the 4-SO4GalNAc was adsorbed through electrostatic interaction on cationic liposomes, which was confirmed by change in zeta potential from +48.2 ± 3.7 mV for Lip to +12.2 ± 1.3 mV for Sulf-Lip. The mean particle size of Sulf-Lip and Man-Lip was found to be 139.4 ± 7.4 nm and 147.4 ± 8.6 nm respectively. Flow cytometric data reveals enhanced uptake of Sulf-Lip in both J774 and RAW cell lines as compared to Man-Lip. Intracellular localization studies indicate that the fluorescence intensity of Sulf-Lip was much higher as compared to Man-Lip and Lip formulations. Sulf-Lip and Man-Lip showed significantly higher localization of AmB at all time points compared to Lip (P<0.05) after i.v. administration. The studies provides evidences that 4-SO4GalNAc possess promising feature for targeting resident macrophages and its application in the conditions of leishmaniasis is in offing.
 
Format 4408836 bytes
application/pdf
 
Language en
 
Relation CDRI communication number 8100
 
Subject 4-sulfated N-acetyl galactosamine
Mannose receptors
Macrophages
Liposomes
 
Title Investigations on Alternate Approach to Target Mannose Receptors on Macrophages using 4-Sulfated N-Acetyl Galactosamine more Efficiently as Compared to Mannose Decorated Liposomes: an Application in Drug Delivery
 
Type Article