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Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis

Osteoarthritis (OA) is a common cause of pain and disability. Local corticosteroid injections are effective in treating OA pain and inflammation but are short-acting. Prolonged intra-articular (IA) corticosteroid exposure may even lead to cartilage deterioration. The aim of this prospective study wa...

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Autores principales: Tellegen, Anna, Beukers, Martijn, Rudnik-Jansen, Imke, van Klaveren, Nicolien, How, Kan Loi, Woike, Nina, Mihov, George, Thies, Jens, Teske, Erik, Creemers, Laura, Tryfonidou, Marianna, Meij, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999265/
https://www.ncbi.nlm.nih.gov/pubmed/33799665
http://dx.doi.org/10.3390/pharmaceutics13030372
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author Tellegen, Anna
Beukers, Martijn
Rudnik-Jansen, Imke
van Klaveren, Nicolien
How, Kan Loi
Woike, Nina
Mihov, George
Thies, Jens
Teske, Erik
Creemers, Laura
Tryfonidou, Marianna
Meij, Björn
author_facet Tellegen, Anna
Beukers, Martijn
Rudnik-Jansen, Imke
van Klaveren, Nicolien
How, Kan Loi
Woike, Nina
Mihov, George
Thies, Jens
Teske, Erik
Creemers, Laura
Tryfonidou, Marianna
Meij, Björn
author_sort Tellegen, Anna
collection PubMed
description Osteoarthritis (OA) is a common cause of pain and disability. Local corticosteroid injections are effective in treating OA pain and inflammation but are short-acting. Prolonged intra-articular (IA) corticosteroid exposure may even lead to cartilage deterioration. The aim of this prospective study was to assess safety and provide proof-of-concept of IA-applied biodegradable polyesteramide-based microspheres (PEAMs) gradually releasing triamcinolone acetonide (TA). Mimicking continuous exposure associated with local drug delivery in canine articular chondrocytes cultured in the continuous presence of TA tissue regeneration was not affected, whereas intermittent exposure reduced proteoglycan production. In this respect, TA-PEAMs administered IA in a proof-of-concept study in 12 client-owned dogs with established OA also showed safety by radiographic examination, without changes in OA severity and in glycosaminoglycan synovial fluid levels. Treatment also resulted in clinical improvement in 10 out of 11 dogs during the two-month follow-up period, which persisted in 6 out of 10 dogs after 6 months, based on objective gait analysis and owner questionnaires. Synovial prostaglandin E(2), a pro-inflammatory marker, was decreased two months after treatment. This study showed safety and proof-of-concept of IA-administered TA-PEAMs in dogs with OA, as a first step towards translation into the veterinary and human clinic.
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spelling pubmed-79992652021-03-28 Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis Tellegen, Anna Beukers, Martijn Rudnik-Jansen, Imke van Klaveren, Nicolien How, Kan Loi Woike, Nina Mihov, George Thies, Jens Teske, Erik Creemers, Laura Tryfonidou, Marianna Meij, Björn Pharmaceutics Article Osteoarthritis (OA) is a common cause of pain and disability. Local corticosteroid injections are effective in treating OA pain and inflammation but are short-acting. Prolonged intra-articular (IA) corticosteroid exposure may even lead to cartilage deterioration. The aim of this prospective study was to assess safety and provide proof-of-concept of IA-applied biodegradable polyesteramide-based microspheres (PEAMs) gradually releasing triamcinolone acetonide (TA). Mimicking continuous exposure associated with local drug delivery in canine articular chondrocytes cultured in the continuous presence of TA tissue regeneration was not affected, whereas intermittent exposure reduced proteoglycan production. In this respect, TA-PEAMs administered IA in a proof-of-concept study in 12 client-owned dogs with established OA also showed safety by radiographic examination, without changes in OA severity and in glycosaminoglycan synovial fluid levels. Treatment also resulted in clinical improvement in 10 out of 11 dogs during the two-month follow-up period, which persisted in 6 out of 10 dogs after 6 months, based on objective gait analysis and owner questionnaires. Synovial prostaglandin E(2), a pro-inflammatory marker, was decreased two months after treatment. This study showed safety and proof-of-concept of IA-administered TA-PEAMs in dogs with OA, as a first step towards translation into the veterinary and human clinic. MDPI 2021-03-11 /pmc/articles/PMC7999265/ /pubmed/33799665 http://dx.doi.org/10.3390/pharmaceutics13030372 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Tellegen, Anna
Beukers, Martijn
Rudnik-Jansen, Imke
van Klaveren, Nicolien
How, Kan Loi
Woike, Nina
Mihov, George
Thies, Jens
Teske, Erik
Creemers, Laura
Tryfonidou, Marianna
Meij, Björn
Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title_full Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title_fullStr Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title_full_unstemmed Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title_short Intra-Articular Slow-Release Triamcinolone Acetonide from Polyesteramide Microspheres as a Treatment for Osteoarthritis
title_sort intra-articular slow-release triamcinolone acetonide from polyesteramide microspheres as a treatment for osteoarthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999265/
https://www.ncbi.nlm.nih.gov/pubmed/33799665
http://dx.doi.org/10.3390/pharmaceutics13030372
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