Synthesis And Evaluation Of Biological Properties Of Derivatives Of Cephalosporins (Record no. 2346)

000 -LEADER
fixed length control field 02141nam a2200193Ia 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20150918143716.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 150525s1999 xx 000 0 und d
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 0602,T
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name Rehmat Ullah, Major
110 ## - MAIN ENTRY--CORPORATE NAME
Location of meeting Dr.Muhammad Sabir
245 ## - TITLE STATEMENT
Title Synthesis And Evaluation Of Biological Properties Of Derivatives Of Cephalosporins
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Year of publication 1999
502 ## - DISSERTATION NOTE
Dissertation note This study was aimed at preparation and evaluation of the biological properties of cephradine. Schiff base transition metal complexes of cephradine were prepared. In the first step Schiff bases were prepared by condensation of the primary amine with a carbonyl compound. For this purpose pyridoxal HCI and salicylaldehyde were used. In the next step the prepared Schiff bases were chelated with metal salts using copper acetate and zinc acetate, here metal binds to polydenate ligands to form the ring structure, where metal is the part of the ring. In this way a three dimensional molecule was obtained which exhibited enhanced antibacterial activity in some cases and depressed activity in the others. The complexes were subjected to biological evaluation to find out the minimum lethal concentration of the new complexes and then it was compared with the parent drug. The standard organisms of S. aureus, .E.coli Pseudomonas aeruginosa and . pneumoniae were used to study the antimicrobial activity. Cephradine complexes showed a depressed activity against S. aureus, . E.coli and P . aemginosa. But the activity of CPC and CSC derivatives was found ten times enhanced against
K. pneumoniae, when compared with the present drug. The haematological study revealed that the parent drug and the new derivatives did not have any deleterious effect upon the total erythrocyte count, haemoglobin concentration, leukocytic count, differential leukocytic count i.e., lymphocytes and polyrnorphs (neutrophils). Thus the new compounds were found to be as safe as the parent drug itself.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Department of Pharmaoclogy & Toxicology
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dr.Haji Ahmad
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dr.Muhammad Raziq Ali
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Holdings
Damaged status Collection code Permanent Location Current Location Shelving location Date acquired Full call number Accession Number Koha item type
  Veterinary Science UVAS Library UVAS Library Thesis Section 2015-05-27 0602,T 0602,T Thesis


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