Literature DB >> 32647102

Hyaluronic acid-coated gold nanorods enhancing BMP-2 peptide delivery for chondrogenesis.

Kanokwan Sansanaphongpricha1, Pacharapan Sonthithai, Pakkanun Kaewkong, Boonlom Thavornyutikarn, Suwussa Bamrungsap, Wasana Kosorn, Tapanee Thinbanmai, Nattika Saengkrit.   

Abstract

Bone morphogenic protein-2 (BMP-2) knuckle epitope peptide has been recently discovered and known to activate chondrogenesis. However, the applications of this soluble peptide remain very limited due to rapid diffusion resulting in poor cellular uptake into target cells. We herein designed nanoparticles made from hyaluronic acid functionalized gold nanorods (GNRs) to conjugate with thiolated BMP-2 knuckle epitope peptide via a two-step reaction. Hyaluronic acid was modified to have thiol functional groups to replace the cetyl trimethylammonium bromide ligands on the surface of GNRs. The thiolated peptides were subsequently reacted with hyaluronic acid on the surface on GNRs via a maleimide-hydrazide crosslinker. The conjugation was confirmed by the change of surface charge of GNRs and the plasmon shift. A colorimetric peptide assay suggested more than 69% of the thiolated peptides were conjugated with the hyaluronic acid coated gold nanorods. Moreover, in vitro cell viability showed that BMP-2 conjugated hyaluronic acid functionalized gold nanorods (B2HGR) were cytocompatible and did not cause cytotoxicity to fibroblast cells. The B2HGRs also significantly promote cellular uptake of the BMP-2 peptides in both human mesenchymal stem cells and porcine chondrocytes due to multivalent ligand binding to the BMP receptors on the cell surface resulting in receptor-mediated endocytosis. The enhanced cellular uptake was clearly observed under a confocal microscope resulting in the significant activation of type II collagen gene expression and glucosaminoglycan secretion in those cells. Furthermore, our delivery system is a proof-of-concept of using scaffolds in combination with nanodelivery platform to enhance cartilaginous repair. The peptide loading capacity and the release is not limited by the scaffolds. Therefore, our delivery platform has potential applications for cartilage regeneration in a preclinical and clinical setting in the future.

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Year:  2020        PMID: 32647102     DOI: 10.1088/1361-6528/aba46d

Source DB:  PubMed          Journal:  Nanotechnology        ISSN: 0957-4484            Impact factor:   3.874


  4 in total

Review 1.  Endocytosis of abiotic nanomaterials and nanobiovectors: Inhibition of membrane trafficking.

Authors:  Pooyan Makvandi; Meiling Chen; Rossella Sartorius; Ali Zarrabi; Milad Ashrafizadeh; Farnaz Dabbagh Moghaddam; Jingzhi Ma; Virgilio Mattoli; Franklin R Tay
Journal:  Nano Today       Date:  2021-09-08       Impact factor: 20.722

Review 2.  The application prospect of metal/metal oxide nanoparticles in the treatment of osteoarthritis.

Authors:  Junchao Luo; Yin Zhang; Senbo Zhu; Yu Tong; Lichen Ji; Wei Zhang; Qiong Zhang; Qing Bi
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2021-08-20       Impact factor: 3.000

3.  Exosome-delivered BMP-2 and polyaspartic acid promotes tendon bone healing in rotator cuff tear via Smad/RUNX2 signaling pathway.

Authors:  Lei Han; Hong Liu; Huajun Fu; Yugen Hu; Weili Fang; Junsheng Liu
Journal:  Bioengineered       Date:  2022-01       Impact factor: 3.269

Review 4.  Gold Nanomaterials and Bone/Cartilage Tissue Engineering: Biomedical Applications and Molecular Mechanisms.

Authors:  Yifeng Shi; Xuyao Han; Shuang Pan; Yuhao Wu; Yuhan Jiang; Jinghao Lin; Yihuang Chen; Haiming Jin
Journal:  Front Chem       Date:  2021-07-09       Impact factor: 5.221

  4 in total

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