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Original
Research Article
Flurbiprofen- and
Suprofen-Dextran Conjugates: Synthesis, Characterization
and Biological Evaluation
Sushant K Shrivastava1*, DK
Jain2, Prabhat K
Shrivastava1, and Piyush Trivedi3
1Department
of Pharmaceutics, Institute of Technology,
Banaras Hindu University, Varanasi, U.P.,
2Department of Pharmacy, IPS
Academy, Indore, M.P., 3School of
Pharmaceutical Sciences, Rajiv Gandhi
Proudyogiki Vishwavidyalaya, Bhopal, M.P.,
India
*For correspondence:
E-mail:
sushant_itbhu@rediffmail.com Tel
+91-543-2307049, Fax+91-542-2368428
Received: 9 Oct
2008
Revised accepted: 15 Dec 2008
Tropical
Journal of Pharmaceutical Research, June 2009; 8(3):
221-229
Abstract
Purpose: To synthesize and characterize
the dextran conjugates of suprofen and flurbiprofen, and
also evaluate their biological activities.
Methods: Suprofen and flurbiprofen were
individually reacted with carbonyldiimidazole to form
acylimidazole, which, in turn, was reacted with the
dextran of varying molecular weight (40 000, 60 000, and
110 000) to form drug-dextran conjugates. The structures
of the synthesized dextran conjugates were confirmed by
IR and NMR spectroscopy. In vitro hydrolysis of the
conjugates were studied in buffer solutions (pH 7.4 and
9.0) and 80% human plasma (pH 7.4). The analgesic and
antipyretic activities, as well as the ulcerogenic index
of the conjugates were also evaluated in albino rats.
Results: The mean degree of
substitution of flurbiprofen and suprofen
was between 8.0 to 9.5
% and 7.5 to 9.0 %, respectively. In vitro hydrolysis
studies on the conjugates indicate faster hydrolysis at
pH 9.0 than in pH 7.4 buffer solution and 80% human
plasma (pH 7.4) with the process following First order
kinetics. The analgesic activity of flurbiprofen-dextran
conjugate (FD-110) suprofen-dextran conjugate (SD-110)
was 64.23 and 41.50% which compare well with those of
their parent drugs - flurbiprofen (72.60%) and suprofen
(44.30%). Similar findings were made in respect of the
antipyretic activity. Both flurbiprofen and suprofen
showed deep ulceration, swelling and high intensity
perforation in the gastric mucosa after seven days
administration of flurbiprofen and suprofen with the
ulcerogenic indices of 29.69 and 31.0 respectively,
cpmpare with 5.88 and 6.06 for FD-110
and SD-110, respectively.
Conclusion:
Dextran can be employed as a pro-moiety or
carrier for the delivery of flurbiprofen and suprofen
and showed comparable analgesic and antipyretic
activities with the parent drugs but with lower
ulcerogenic indices.
Keywords: Flurbiprofen, Suprofen,
Dextran conjugates, In vitro hydrolysis,
Analgesic-antipyretic activity |