Novel Injectable Fluorescent Polymeric Nanocarriers for Intervertebral Disc Application

Author:

Arul Michael R.1,Zhang Changli2ORCID,Alahmadi Ibtihal3,Moss Isaac L.1,Banasavadi-Siddegowda Yeshavanth Kumar4ORCID,Abdulmalik Sama1,Illien-Junger Svenja2ORCID,Kumbar Sangamesh G.135ORCID

Affiliation:

1. Department of Orthopedic Surgery, University of Connecticut Health, Farmington, CT 06030, USA

2. Department of Orthopedic Surgery, Emory University, Atlanta, GA 30308, USA

3. Department of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA

4. Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA

5. Department of Materials Science and Engineering, University of Connecticut, Storrs, CT 06269, USA

Abstract

Damage to intervertebral discs (IVD) can lead to chronic pain and disability, and no current treatments can fully restore their function. Some non-surgical treatments have shown promise; however, these approaches are generally limited by burst release and poor localization of diverse molecules. In this proof-of-concept study, we developed a nanoparticle (NP) delivery system to efficiently deliver high- and low-solubility drug molecules. Nanoparticles of cellulose acetate and polycaprolactone-polyethylene glycol conjugated with 1-oxo-1H-pyrido [2,1-b][1,3]benzoxazole-3-carboxylic acid (PBC), a novel fluorescent dye, were prepared by the oil-in-water emulsion. Two drugs, a water insoluble indomethacin (IND) and a water soluble 4-aminopyridine (4-AP), were used to study their release patterns. Electron microscopy confirmed the spherical nature and rough surface of nanoparticles. The particle size analysis revealed a hydrodynamic radius ranging ~150–162 nm based on dynamic light scattering. Zeta potential increased with PBC conjugation implying their enhanced stability. IND encapsulation efficiency was almost 3-fold higher than 4-AP, with release lasting up to 4 days, signifying enhanced solubility, while the release of 4-AP continued for up to 7 days. Nanoparticles and their drug formulations did not show any apparent cytotoxicity and were taken up by human IVD nucleus pulposus cells. When injected into coccygeal mouse IVDs in vivo, the nanoparticles remained within the nucleus pulposus cells and the injection site of the nucleus pulposus and annulus fibrosus of the IVD. These fluorescent nano-formulations may serve as a platform technology to deliver therapeutic agents to IVDs and other tissues that require localized drug injections.

Funder

National Institutes of Biomedical Imaging and Bioengineering

U.S. Army Medical Research Acquisition Activity

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

MDPI AG

Subject

Biomedical Engineering,Biomaterials

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