Targeted treatment for osteoarthritis: drugs and delivery system

Drug Deliv. 2021 Dec;28(1):1861-1876. doi: 10.1080/10717544.2021.1971798.

Abstract

The management of osteoarthritis (OA) is a clinical challenge due to the particular avascular, dense, and occluded tissue structure. Despite numerous clinical reports and animal studies, the pathogenesis and progression of OA are still not fully understood. On the basis of traditional drugs, a large number of new drugs have been continuously developed. Intra-articular (IA) administration for OA hastens the development of targeted drug delivery systems (DDS). OA drugs modification and the synthesis of bioadaptive carriers contribute to a qualitative leap in the efficacy of IA treatment. Nanoparticles (NPs) are demonstrated credible improvement of drug penetration and retention in OA. Targeted nanomaterial delivery systems show the prominent biocompatibility and drug loading-release ability. This article reviews different drugs and nanomaterial delivery systems for IA treatment of OA, in an attempt to resolve the inconsonance between in vitro and in vivo release, and explore more interactions between drugs and nanocarriers, so as to open up new horizons for the treatment of OA.

Keywords: Osteoarthritis; drug delivery system; intra-articular treatment; nanoparticles; targeted treatment.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Hormones / pharmacology
  • Adrenal Cortex Hormones / therapeutic use
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Cartilage / drug effects
  • Chondrocytes / drug effects
  • Drug Carriers
  • Drug Combinations
  • Drug Liberation
  • Drugs, Chinese Herbal / pharmacology
  • Drugs, Chinese Herbal / toxicity
  • Gene Transfer Techniques
  • Genetic Therapy / methods
  • Humans
  • Inflammation Mediators / administration & dosage
  • Inflammation Mediators / pharmacology
  • Inflammation Mediators / therapeutic use
  • Injections, Intra-Articular
  • Nanoparticles / chemistry
  • Osteoarthritis / drug therapy*
  • Osteoarthritis / physiopathology*
  • Osteoarthritis / therapy
  • Reactive Oxygen Species / metabolism
  • Synovial Membrane / drug effects

Substances

  • Adrenal Cortex Hormones
  • Anti-Inflammatory Agents, Non-Steroidal
  • Drug Carriers
  • Drug Combinations
  • Drugs, Chinese Herbal
  • Inflammation Mediators
  • Reactive Oxygen Species

Grants and funding

This work was supported by National Natural Science Foundation of China [NO. 81871835] and Shanghai Key Laboratory of Human Sport Competence Development and Maintenance (Shanghai University of Sport) [NO. 11DZ2261100].