J. Szymura-oleksiak et al., The kinetics of pentoxifylline release in vivo from drug-loaded hydroxyapatite implants, CERAM INT, 27(7), 2001, pp. 767-772
Porous hydroxyapatite implants were evaluated as potential skeletal deliver
y systems for sustained delivery of drugs. Pentoxifylline (PTX) was employe
d as a model agent and 50 mg of PTX powder was loaded into hollow cylindric
al implants. The kinetics of PTX release from the implants was studied both
in vitro, employing phosphate buffer (pH 7.35) at the temperature of 37 de
greesC, and in vivo, implanting drug-containing cylinders into rabbit iliac
bones. For the sake of comparison rabbits were also administered a single
i.v. or i.m. dose of 50 mg PTX. Serum PTX concentration levels were measure
d using the HPLC method. Results of analyses carried out employing the merc
ury porosimetry method and the hydrostatic weighing method showed that the
investigated biomaterial was characterized by a large number of pores rangi
ng in size from 0.4 to 6 mum and with open and total porosity values of 31.
8 and 35.6%. respectively. Studies in vitro revealed typical sigmoid-type d
rug release patterns with a lag time. After 40 h, the amount of released PT
X reached a plateau and equaled 78% of the total amount of drug loaded into
an implant. Studies in vivo demonstrated that due to decelerated PTX relea
se from cylinders implanted in rabbit iliac bones. its serum concentration
values were maintained at measurable levels almost eight times longer than
following the systemic administration of PTX. The serum half-life following
PTX administration via implants was significantly higher than the value ca
lculated after systemic administration and equaled 6.3 h. The authors also
showed that despite differences in the temporal distribution of PTX concent
ration values, its bioavailability was similar after i.m. injections and ad
ministration via implants. As it follows from the investigations. hydroxyap
atite implants manifest positive drug-release patterns both in vitro and in
vivo. (C) 2001 Elsevier Science Ltd and Techna S.r.l. All rights reserved.