ANNUAL REPORT - Department of Biotechnology
ANNUAL REPORT - Department of Biotechnology
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.