Computed Tomography Imaging and Characteristics of In Situ Forming Implants with Different PLGA Endcaps

A poly(lactic-co-glycolic acid) (PLGA)-based in situ-forming implant (ISFI) is a long-acting injectable composed of active ingredients, a biodegradable polymer and a biocompatible solvent. Understanding the role of PLGA end-caps is crucial for designing ISFI formulations due to their impact on drug delivery performance. In this study, using leuprolide acetate as a model drug, we characterized the ISFIs using computed tomography (CT) imaging to explore the influence of PLGA end-cap on the implant’s formation and drug-release behavior. CT imaging enabled a detailed characterization of implant morphology and internal structure, providing new insights into the relationship between phase inversion, implant formation, and in vitro release performance. Acid-ended PLGA showed a higher initial burst release with 100% of the solvent released at 9 days and a faster release duration of the drug in the in vitro release profile. In contrast, ester-ended PLGA showed a more prolonged release profile, with the plateau phase not reached until approximately day 50. Morphological analysis from CT images of the in vitro implants revealed that acid-ended PLGA formed spherical implants with a dense outer layer, whereas ester-ended PLGA resulted in irregular shapes with a larger size expansion. In vivo CT imaging confirmed these trends, although implant evolution occurred more rapidly in biological environments. Overall, this research highlights the impact of PLGA end-caps on the performance of ISFI, providing a scientific basis for formulation development, evaluation, and optimization of ISFIs.

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Publication Details

Journal
Chemical & Biomedical Imaging
Published
2026-02-17
DOI
https://doi.org/10.1021/cbmi.6c00001
Citations
1
Primary Topic
Advanced Drug Delivery Systems
Type
article
Field-Weighted Citation Impact
27.80
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article

Computed Tomography Imaging and Characteristics of In Situ Forming Implants with Different PLGA Endcaps

Qiangnan Zhang, André O’Reilly Beringhs, Hong Yuan, Seyyed Majid Eslami et al.
1 citations
Chemical & Biomedical Imaging
Advanced Drug Delivery Systems
27.80
article

Computed Tomography Imaging and Characteristics of In Situ Forming Implants with Different PLGA Endcaps

Qiangnan Zhang, André O’Reilly Beringhs, Hong Yuan, Seyyed Majid Eslami, Francis K. Masese, Rajeswari M. Kasi, Bin Qin, Nour N Al Zouabi, L. Ward, Zixuan Zhen, Sheyda Ranjbar, Qi Li, Xiuling Lu, Xinhao Lin, Yan Wang
article en
1 citations

Abstract

A poly(lactic-co-glycolic acid) (PLGA)-based in situ-forming implant (ISFI) is a long-acting injectable composed of active ingredients, a biodegradable polymer and a biocompatible solvent. Understanding the role of PLGA end-caps is crucial for designing ISFI formulations due to their impact on drug delivery performance. In this study, using leuprolide acetate as a model drug, we characterized the ISFIs using computed tomography (CT) imaging to explore the influence of PLGA end-cap on the implant’s formation and drug-release behavior. CT imaging enabled a detailed characterization of implant morphology and internal structure, providing new insights into the relationship between phase inversion, implant formation, and in vitro release performance. Acid-ended PLGA showed a higher initial burst release with 100% of the solvent released at 9 days and a faster release duration of the drug in the in vitro release profile. In contrast, ester-ended PLGA showed a more prolonged release profile, with the plateau phase not reached until approximately day 50. Morphological analysis from CT images of the in vitro implants revealed that acid-ended PLGA formed spherical implants with a dense outer layer, whereas ester-ended PLGA resulted in irregular shapes with a larger size expansion. In vivo CT imaging confirmed these trends, although implant evolution occurred more rapidly in biological environments. Overall, this research highlights the impact of PLGA end-caps on the performance of ISFI, providing a scientific basis for formulation development, evaluation, and optimization of ISFIs.

Chemical & Biomedical Imaging
University of North Carolina at Chapel Hill (US), Center for Drug Evaluation and Research (US), Laboratoire d’Imagerie Biomédicale (FR), Food and Drug Administration (TH)
Openalex Percentile: Top 1%
Advanced Drug Delivery Systems
27.80
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