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Yadav, A. B.

Publications and source records attributed to Yadav, A. B..

2 recordsLinked to original sources

Bioengineered ciprofloxacin loaded chitosan nanoparticles for the treatment of Bovine Mastitis

Mastitis is the most devastating economic disease of dairy cattle. Mastitis in dairy cattle frequently occurs during the dry period or in early lactation. E. coli. and S. aureus is the main causative agent of mastitis. S. aureus has an ability to form encapsulated focuses in the udder and develop subclinical form of mastitis. This property of bacteria hinders the effective cure during lactation period. Antibiotics used for treatments have a short half-life span at the site of action because of frequent milking, therefore unable to maintain desired drug concentration for effective clearance of bacteria. We demonstrated the potential of ciprofloxacin encapsulated nanocarriers which can improve availability of drugs and could provide effective means of the treatment of mastitis. These drug loaded nanoparticles show low toxicity & slow clearance from the site of action. Antimicrobial studied against clinical strain of E.coli. and Staphylococcus aureus zone of inhibition depend on dose 0.5 mg to 2 mg/ml nanoparticles solution from 11.6 to 14.5 mm and 15 to 18mm. These nanoparticles show good antimicrobial activity in broth culture as well against bacteria.

pharmacology and toxicology

Protein stability and functional activity during nebulization: A comparative study of three nebulizer!

Delivery of therapeutics protein to the lung offers effective treatments of lungs disease. Efficacy of delivered therapeutics molecules depends on integrity and stability of protein during nebulization. In this study, we compared three nebulizers: compressed air nebulizer (CAN), ultrasonic nebulizer (USN) and mesh nebulizer (MAN) to deliver aerosol dose, stability and functional activity of a model protein lysozyme. Lysozyme/BSA delivered dose assessed by indirect and direct method. It was shown CAN deliver 0.142{+/-}0.027 to 0.632{+/-} 0.09 ml of protein, USN deliver 0.511{+/-}0.119 to 1.688{+/-}0.173 ml and MAN deliver 0.238{+/-}0.006 to 0.731{+/-}0.013 ml of protein in the same time. Integrity of nebulized proteins were assessed by gel electrophoresis and circular diochorism. It was found integrity of lysozyme compromised in all three nebulizer maximum in CAN and minimum with MAN. The functional activity of protein was assessed after nebulization by turbidometry assay. The functional activity was compromised by all three nebulizer upto some extent. In conclusion, nebulization compromise protein stability: this impact depend on nebulization techniques as well as nature of protein. The CAN deliver protein more precisely in small amount in comparison to the other nebulizer. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=122 SRC="FIGDIR/small/085720v1_ufig1.gif" ALT="Figure 1"> View larger version (30K): org.highwire.dtl.DTLVardef@5b230forg.highwire.dtl.DTLVardef@15ac79corg.highwire.dtl.DTLVardef@e7130forg.highwire.dtl.DTLVardef@94684e_HPS_FORMAT_FIGEXP M_FIG Graphical Abstract C_FIG

bioengineering