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In vitro-in vivo correlation (IVIVC) analysis reveals a relationship between in vitro release and in vivo pharmacokinetic response of the drug of interest. Sandostatin LAR Depot (SLD) for endocrine tumors and acromegaly is a sustained-release formulation of octreotide, a cyclic oligomer of 8 amino acids, which prolongs therapeutic efficacy and enhances medication compliance of octreotide. Since the efficacy of SLD is dependent on the pharmacokinetic characteristics of octreotide released from a biodegradable matrix polymer, poly(lactide-co-glycolide)-glucose, of SLD, the IVIVC of SLD is critical for predicting an in vivo behavior of the octreotide. In this study, in vitro release of octreotide from SLD was investigated using the release test media each containing 0.02% or 0.5% surfactant and having different pH values of 7.4 and 5.5. In vivo pharmacokinetic profiles of SLD were determined by LC-MS/MS analysis of the systemic blood concentration of octreotide after the SLD injection to rodents. In IVIVC analysis, the Weibull model was adopted as a drug release model for biodegradable microsphere formulation. The IVIVC analyses revealed the in vitro release test condition of SLD with the highest IVIV correlation coefficient. By applying the in vitro release data to the model derived from the IVIVC analysis, pharmacokinetic parameters of SLD could be predicted with the prediction error of ± 10 ~ 15%. IVIVC analysis and pharmacokinetic prediction model of SLD in our study can be an efficient tool for the development of long-acting pharmaceutical dosage forms.
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http://dx.doi.org/10.1208/s12249-022-02359-w | DOI Listing |
Turk J Pharm Sci
September 2025
University of Maryland, Department of Pharmaceutical Sciences, Baltimore, USA.
Objectives: Norvir oral powder [ritonavir (RTV)] employs polyvinylpyrrolidone/vinyl acetate as the polymer to formulate an amorphous solid dispersion. Its oral absolute bioavailability is 70% in the fasted state, and it has negative food effects. The aim of this study was to perform in vitro dissolution of Norvir powder and Wagner-Nelson deconvolution of data under fasted, moderate fat, and high fat conditions in order to elucidate the relevance of dissolution testing.
View Article and Find Full Text PDFMol Pharm
September 2025
Boehringer Ingelheim (China) Investment Co., Ltd., 257 Li Shizhen Road, Shanghai 201203, China.
Traditional methods for developing modified-release (MR) formulations involve numerous iterations and large quantities of drug substances, which pose considerable challenges in exploration settings. Given the growing necessity for modified-release (MR) formulations in the pharmaceutical industry, particularly during the preclinical research and development phase, modified-release strategies may serve as attractive alternatives to discontinuing clinical development and could mitigate the costs and time associated with identifying new drug candidates. This study specifically explores the application of melt extrusion deposition (MED) 3D printing technology as a rapid prototyping platform for creating extended-release (ER) oral dosage forms tailored for the preclinical phase.
View Article and Find Full Text PDFPharmacol Res
July 2025
National Institutes for Food and Drug Control, State Key Laboratory of Drug Regulatory Science, Beijing 100050, China. Electronic address:
In recent years, global consumption of seaweed has been on the rise, yet there is a lack of accurate methods for assessing the health risks associated with its consumption. This gap could pose a threat to public safety or lead to wasted resources by government regulatory bodies. In this study, animal models and an innovative PBET (IPBET) were used to determine the bioavailability and bioaccessibility of arsenic (As) and cadmium (Cd) in various seaweeds, followed by an in vivo-in vitro correlation (IVIVC) analysis.
View Article and Find Full Text PDFInt J Pharm
September 2025
College of Pharmaceutical Sciences, Soochow University, Suzhou 215123, People's Republic of China. Electronic address:
Polymeric acids and their copolymer-based microspheres constitute a critical platform for extended and controlled-release drug delivery systems. However, the precipitated drug crystals (commonly termed "quick sand" phenomenon) during microsphere fabrication significantly limits their application for specific drug molecules, leading to suboptimal drug loading (DL) and encapsulation efficiency (EE) in final products. In this study, dezocine-loaded microspheres (Dez-Ms) were fabricated using microfluidic reactor technology.
View Article and Find Full Text PDFNanotheranostics
June 2025
Department of Pharmaceutical Technology, AU College of Pharmaceutical Science, Andhra University, Visakhapatnam, Andhra Pradesh 530003, India.
The present study aimed to overcome the drawbacks of tapentadol through the oral route and to assess the significance of microemulsion gels for transdermal delivery via pharmacokinetic approach. Microemulsions were prepared via a ternary phase diagram. The optimized microemulsion was converted into gels, and the microemulsion was evaluated for particle size, zeta potential and cumulative drug release, whereas the gel was characterized for viscosity, spreadability, , , and skin irritation studies.
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