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

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...

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Published inJournal of pharmaceutical sciences Vol. 105; no. 6; pp. 1934 - 1946
Main Authors You, Siming, Yang, Zichao, Wang, Chi-Hwa
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.06.2016
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Online AccessGet full text
ISSN0022-3549
1520-6017
1520-6017
DOI10.1016/j.xphs.2016.04.002

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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.
AbstractList 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.
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.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.
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.
Author Yang, Zichao
Wang, Chi-Hwa
You, Siming
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Issue 6
Keywords CPP
sensitivity analysis
polymer microspheres
CDM-mLT
drug delivery
CDM
SA
BSA
controlled release
erosion kinetics
TMA-Tyr
TEG
DOE
drug carrier design
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Snippet 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...
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SubjectTerms controlled release
Delayed-Action Preparations - pharmacokinetics
drug carrier design
drug delivery
Drug Liberation
erosion kinetics
Kinetics
Microspheres
Pharmaceutical Preparations - metabolism
polymer microspheres
Polymers - pharmacokinetics
sensitivity analysis
Title Toward Understanding Drug Release From Biodegradable Polymer Microspheres of Different Erosion Kinetics Modes
URI https://dx.doi.org/10.1016/j.xphs.2016.04.002
https://www.ncbi.nlm.nih.gov/pubmed/27238490
https://www.proquest.com/docview/1792772833
Volume 105
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