Abstract:

Abstract： Objective To study the optimum condition of preparing ofloxaxcin gelatin microspheres. Methods Oflox⁃
axcin gelatin microspheres were manufactured using the emulsion chemical-cross linking method and gelatin was employed
as carrier, liquid paraffin as oil phase, Span80 as emulsifier, . The loading capability and entrapment efficiency of the ofloxax⁃
cin gelatin microspheres were determined by UV Spectrophotometry. The effect of gelatin concentration, oil / water volume ra⁃
tio, gelatin/ofloxaxcin mass ratio and volume fraction of span80 on drug loading capability and entrapment efficiency were in⁃
vestigated. The optimum proportions of each component was obtained by L9 (34) orthogonal test, based on the above 4 factors,
using sum of drug loading capability and entrapment efficiency as evaluation index. Results The optimum condition for
manufacturing high quality ofloxaxcin gelatin microspheres used 20% of gelatin concentration， water/oil volume ratio at 3.5∶ 1,
gelatin/ofloxaxcin mass ratio at 1∶1, the span 80 volume fraction of 2.5%. Conclusion Drug loading capability and entrap⁃
ment efficiency of the ofloxaxcin gelatin microspheres reached 80％ using this manufacture technology therefore the prepara⁃
tion was stable and feasible.

Key words: Ofloxaxcin, polygeline, microspheres, technology, pharmaceutical, drug carriers, drug evaluation