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Biodegradable Microspheres and Hydrogel Drug Delivery System of Tumor Necrosis Factor (TNF) Inhibitor and Growth Differentiation Factor 5 (GDF5) Reduces Disk Inflammation in the Rabbit Model.
Yuan, Bo; Rudeen, Kayla; Li, Jun; Williams, Brandon; Sumughan, Saurav; Lopez, Gregory; An, Howard S; Kang-Mieler, Jennifer J; Chee, Ana V.
Afiliación
  • Yuan B; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL.
  • Rudeen K; Department of Orthopaedics, Shanghai Changzheng Hospital, Second Affiliated Hospital of Naval Medical University, Shanghai, China.
  • Li J; Department of Biomedical Engineering, Illinois Institute of Technology, Chicago, IL.
  • Williams B; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL.
  • Sumughan S; Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Lopez G; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL.
  • An HS; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL.
  • Kang-Mieler JJ; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.
  • Chee AV; Department of Orthopedic Surgery, Rush University Medical Center, Chicago, IL.
Spine (Phila Pa 1976) ; 48(15): E257-E265, 2023 Aug 01.
Article en En | MEDLINE | ID: mdl-37075330
STUDY DESIGN: Preclinical study. OBJECTIVE: Develop and test a drug delivery system (DDS) composed of anti-inflammatories and growth factors in the rabbit disk injury model. SUMMARY OF BACKGROUND DATA: Biological therapies that inhibit inflammation or enhance cell proliferation can alter intervertebral disk (IVD) homeostasis to favor regeneration. As biological molecules have short half-lives and one molecule may not cover multiple disease pathways, effective treatments may require a combination of growth factors and anti-inflammatory agents delivered in a sustained manner. MATERIALS AND METHODS: Biodegradable microspheres were generated separately to encapsulate tumor necrosis factor alpha (TNFα) inhibitors [etanercept (ETN)] or growth differentiation factor 5 (GDF5) and were embedded into a thermoresponsive hydrogel. Release kinetics and activity of ETN and GDF5 were measured in vitro . For in vivo testing, New Zealand White rabbits (n=12) underwent surgery for disk puncture and treatment with blank-DDS, ETN-DDS, or ETN+GDF5-DDS at levels L34, L45, and L56. Radiographic and magnetic resonance images of the spines were obtained. The IVDs were isolated for histologic and gene expression analyses. RESULTS: ETN and GDF5 were encapsulated into poly (L-lactide-co-glycolide) microspheres and had average initial bursts of 2.4±0.1 and 11.2±0.7 µg from DDS, respectively. In vitro studies confirmed that ETN-DDS inhibited TNFα-induced cytokine release and GDF5-DDS induced protein phosphorylation. In vivo studies showed that rabbit IVDs treated with ETN+GDF5-DDS had better histologic outcomes, higher levels of extracellular, and lower levels of inflammatory gene expression than IVDs treated with blank-DDS or ETN-DDS. CONCLUSIONS: This pilot study demonstrated that DDS can be fabricated to deliver sustained and therapeutic dosages of ETN and GDF5. In addition, ETN+GDF5-DDS may have greater anti-inflammatory and regenerative effects than ETN-DDS alone. Thus, intradiscal injection of controlled release TNF-α inhibitors and growth factors may be a promising treatment to reduce disk inflammation and back pain.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor de Necrosis Tumoral alfa / Inhibidores del Factor de Necrosis Tumoral Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Spine (Phila Pa 1976) Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor de Necrosis Tumoral alfa / Inhibidores del Factor de Necrosis Tumoral Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Spine (Phila Pa 1976) Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos