இரசாயன பொறியியல் மற்றும் செயல்முறை தொழில்நுட்ப இதழ்
திறந்த அணுகல்

சுருக்கம்

A rare class of poly (sugar acids): Poly [3-(3, 4-dihydroxyphenyl) glyceric acid] from medicinal plants of boraginaceae family and its anticancer efficacy

Barbakadze V

Natural polysaccharides have long been studied and widely used in medicine and pharmaceutics. Besides, within the field of pharmacologically active biopolymers the area of stable polyethers seems rather new and attractive. The main chemical constituent of high molecular (>1000 kDa) water-soluble preparations from medicinal plants of Symphytum asperum, S.caucasicum, S.officinale, S.grandiflorum, Anchusa italica, Cynoglossum officinale and Borago officinalis (Boraginaceae) according to data of liquid-state 1H, 13C NMR, 2D 1H/13C HSQC, 2D DOSY and solid-state 13C NMR spectra was found to be poly[oxy-1-carboxy-2-(3,4-dihydroxyphenyl) ethylene] or poly[3-(3,4-dihydroxyphenyl)glyceric acid] (PDPGA). The polyoxyethylene chain is the backbone of this biopolymer. 3, 4-Dihydroxyphenyl and carboxyl groups are regular substituents at two carbon atoms in the chain. The repeating unit of this regular polyether is 3-(3, 4-dihydroxyphenyl) glyceric acid residue. PDPGA as a 3,4-dihydroxyphenyl derivative of poly(2,3-glyceric acid ether) belongs to a rare class of poly(sugar acids) as well. Its basic monomeric moiety glyceric acid is oxidative form of aldotriose glyceraldehyde. In this case poly (2, 3-glyceric acid ether) chain is the backbone of this polymer molecule and 3,4-dihydroxyphenyl groups are regular substituents at 3C carbon atoms in the chain. Every repeating structural unit of a unique PDPGA contains two phenolic hydroxyl groups in ortho-position and one carboxyl group. Multifunctionality of PDPGA should be a reason of its wide spectrum of biological activities. Oligomers of PDPGA was synthesized by “green” chemistry enzymatic ring opening polymerisation of methyl 3-(3, 4-dibenzyloxyphenyl) glycidate using lipase from Candida rugosa and further deprotections. Enzymatically obtained oligomers cause interest for diverse biological tests. PDPGA exerted anticancer activity in vitro and in vivo against androgen-dependent and -independent human prostate cancer (PCA) cells via targeting androgen receptor, cell cycle arrest and apoptosis without any toxicity, together with a strong decrease (87%) in prostate specific antigen level in plasma. Thus, PDPGA was identified as a potent agent against PCA without any toxicity.