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ANNUAL REPORT - Department of Biotechnology

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Cross Sectional Morphology <strong>of</strong> the TPHSM Impregnated Collagen<br />

delivery device is one such class <strong>of</strong> new generation<br />

wound dressing.<br />

Drug Development<br />

Investigations on programmed cell death in<br />

pathogenic bacteria: towards developing novel<br />

antibiotics to control infectious diseases were carried<br />

out at JNU, New Delhi. The organism under study,<br />

Bacillus anthracis, is a pathogen that causes deadly<br />

anthrax disease in cattle and humans. Through<br />

extensive database mining and BLAST search, a<br />

Toxin-Antitoxin module has been hypothesized in B.<br />

anthracis chromosomal DNA where it exists as an<br />

operon and was found to be 50% homologous to E.<br />

coli. The toxin is reported to belong to a family <strong>of</strong><br />

PemK like toxins (116 amino acid residues) while the<br />

antitoxin (95 amino acid residues) is not well defined<br />

in the database. The genetic organization <strong>of</strong> toxinantitoxin<br />

loci led the investigation to infer the<br />

presence <strong>of</strong> second ORF upstream from the PemK<br />

DBT Annual Report 2006-07<br />

110<br />

homolog <strong>of</strong> B. anthracis.<br />

Drug Delivery<br />

Studies on drug delivery system targeting <strong>of</strong> antileishmanial<br />

drugs to specific sites using lipid<br />

microspheres were carried out at Kakatiya University,<br />

Warangal & IICB, Kolkata. The pharmacokinetic<br />

parameters <strong>of</strong> Amphotericin B in rats and mice were<br />

influenced by the type <strong>of</strong> lipid microspheres<br />

formulation administered. Pegylated lipid<br />

microspheres exhibited higher mean residence time<br />

while mannose grafted and positively charged<br />

systems cleared quickly due to rapid tissue<br />

distribution. Tissue distribution studies revealed the<br />

facts that both the mannose grafted lipid<br />

microspheres and positively charged lipid<br />

microsphers are concentrated in liver and spleen<br />

where the leishmania parasite resides. This is in<br />

conformity with the results obtained in in vivo antileishmanial<br />

studies. The nephrotoxicity observed is<br />

due to high Amphotericin B levels in kidneys following<br />

fungizone administration. Amphotericin B distribution<br />

to kidney and brain has not been influenced much by<br />

the type <strong>of</strong> formulation administered. The<br />

pharmacokinetic parameters obtained both in rats<br />

and mice with piperine followed similar pattern. The<br />

clearance was very high for free piperine as<br />

compared to those obtained following the<br />

administration <strong>of</strong> formulations. The tissue distribution<br />

pattern <strong>of</strong> piperine following the IV administration <strong>of</strong><br />

free piperine and lipid microspheres formulations is<br />

similar to that <strong>of</strong> Amphotericin B indicating the strong<br />

influence <strong>of</strong> the characters <strong>of</strong> the lipid microspheres<br />

on drug distribution.<br />

Acanthamoeba<br />

Studies continued on in vitro pathogenicity, molecular<br />

characterization and molecular diagnosis <strong>of</strong><br />

Acanthamoeba infections at LVPEI & CCMB,<br />

Hyderabad. Results <strong>of</strong> the assay done on clinical<br />

samples from test and control subjects were found to<br />

have a sensitivity <strong>of</strong> >85.0% with some <strong>of</strong> the<br />

smear/culture positive samples failing to amplify the<br />

Acanthamoeba specific amplicons.

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