Title:Chondromodulating Chimeric Prodrugs of Diacetylrhein: Synthesis and Evaluation in Monoiodoacetate-induced Hyperalgesia
Volume: 9
Issue: 3
Author(s): Suneela Dhaneshwar and Dipmala Patil
Affiliation:
Keywords:
Chimeric prodrugs, Diacetylrhein, Essential amino acids, IL-1 inhibitor, Monoiodoacetate-induced hyperalgesia,
Osteoarthritis, Ulcerogenicity, hyaluronic acid, D-phenylalanine, L-tryptophan
Abstract: Chondromodulating chimeric prodrugs of diacetylrhein were synthesized with an objective of potentiating its
moderate anti-inflammatory effect and optimizing its hydrophilic/lipophilic balance by conjugating it with essential amino
acids through a bioreversible amide linkage. In vitro release in HCl buffer (pH 1.2) showed insignificant release of diacetylrhein.
However in phosphate buffer (pH 7.4), almost complete release of diacetylrhein was attained over a period of 4.5
h, following first order kinetics. The prodrug was screened extensively for therapeutic efficacy in monoiodoacetateinduced
rat hyperalgesia model for levels of various markers of osteoarthritis, knee diameter and locomotor activity over a
period of three months. Amongst the three prodrugs synthesized, diacetylrhein-L-tryptophan prodrug exhibited highest activity
by reducing knee diameter, serum alkaline phosphatase and serum glucosaminoglycan to the baseline levels while
increasing the spontaneous locomotor activity. It was found to provide maximum protection against Freund’s adjuvant arthritis
with minimum ulcerogenic potential and better chondroprotection than diacetylrhein.
