Wp. Hu et al., SYNTHESIS AND CHARACTERIZATION OF METHACRYLIC DERIVATIVES AS DRUG CARRIERS, Drug development and industrial pharmacy, 23(7), 1997, pp. 671-678
p-Methoxyphenyl methacrylate (ESMAA) was copolymerized with methacryli
c acid (MAA) in dioxane solutions using azobisisobutyronitrile (AIBN)
as an initiator. The compositions of the copolymers were assayed for t
he aromatic ester content by measuring the ultraviolet (UV) absorbance
at 240 nm in dioxane. The monomer reactivity ratios r(1) and r(2) for
copolymerization of MAA(M-1) and ESMAA(M-2) are 1.52 and 3.01. The gl
ass transition temperatures of MAA-ESMAA copolymers are almost equal t
o the weight-average values. The drug released from copolymers increas
es with the composition of methacrylic acid units. The releases of pir
oxicam from the MAA-co-ESMAA matrices containing 55 mole% MAA in pH 7.
4 and 10 buffer solutions are steady for the whole release period, and
release profiles matches closely to the disintegration profiles of th
e MAA-55 copolymer.