Toward Understanding Drug Release From Biodegradable Polymer Microspheres of Different Erosion Kinetics Modes.

Abstract:

:Two generalized modes of erosion kinetics, that is, the power law mode and root type mode, respectively, were found to be able to better describe the reported weight loss data compared to the existing linear mode, for commonly used surface-eroding polymer microspheres. Based on the newly identified modes, a set of drug release models were developed by extending the existing model. Model validation was achieved by comparing the model predictions to the reported experimental data for surface-eroding polymer microspheres (poly(ortho esters) and polyanhydrides), and good consistency was found. Parameter investigation was conducted to reveal the effects of various important parameters (the dimensionless ratio between diffusion and erosion rates (Er), the dimensionless ratio between erosion and dissolution rates (p), the dimensionless drug loading concentration (q), and the fitting parameter of erosion kinetics (a)) on drug release behavior, which has rarely been examined previously. In general, the effects of these parameters were more significant for an earlier stage, and p, q, and a could effectively vary the drug release percentage. Design-of-experiments-based sensitivity analysis was further carried out and it was found that the most sensitive parameters were p (2.97%) and q (2.97%) for the cases of the power law mode, while it was a (-7.07%) for the cases of the root type mode. The information from the parameter investigation and sensitivity analysis could serve as a straightforward data bank for the practical designing of drug delivery processes. The proposed models are potential mathematical frameworks for the designing of drugs that are based on surface-eroding polymer microspheres in the future.

journal_name

J Pharm Sci

authors

You S,Yang Z,Wang CH

doi

10.1016/j.xphs.2016.04.002

subject

Has Abstract

pub_date

2016-06-01 00:00:00

pages

1934-1946

issue

6

eissn

0022-3549

issn

1520-6017

pii

S0022-3549(16)41370-5

journal_volume

105

pub_type

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