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REVIEW

The Emerging Roles of Nanocarrier Drug Delivery System in Treatment of Intervertebral Disc Degeneration-Current Knowledge, Hot Spots, Challenges and Future Perspectives

, , , &
Pages 1007-1022 | Received 08 Nov 2023, Accepted 09 Mar 2024, Published online: 29 Mar 2024

Figures & data

Figure 1 A diagram showing healthy IVD and the key pathogenic and anatomical alterations in IVDD. MMPs is Matrix metalloproteinases, ADAMTS is Metalloproteinase with Thrombospondin Motif.

Figure 1 A diagram showing healthy IVD and the key pathogenic and anatomical alterations in IVDD. MMPs is Matrix metalloproteinases, ADAMTS is Metalloproteinase with Thrombospondin Motif.

Figure 2 Diagnostic methods and current treatments of LDH.

Figure 2 Diagnostic methods and current treatments of LDH.

Table 1 Main Nano-Drug Delivery Systems for IVDD

Figure 3 NDDSs that are commonly used for IVDD therapy.

Figure 3 NDDSs that are commonly used for IVDD therapy.

Table 2 Recently Representative Research of Nano-Drug Delivery Systems for Treatment of IVDD

Table 3 Representative Exosome Transferred miRNAs in Treatment of IVDD

Figure 4 Exosome and miRNA biogenesis. (A) Exosome biogenesis. (B). Exosome composition. (C). Exosome internalization. (D) miRNA biogenesis; Pol II is an RNA polymerase II, whereas RNAP III is an RNA polymerase III.

Figure 4 Exosome and miRNA biogenesis. (A) Exosome biogenesis. (B). Exosome composition. (C). Exosome internalization. (D) miRNA biogenesis; Pol II is an RNA polymerase II, whereas RNAP III is an RNA polymerase III.

Figure 5 Therapeutic molecules (miRNAs) transferred by MSC-derived exosomes in treatment of IVDD. (A) Schematic representation of an experimental intradiscal injection of MSC-derived exosomes in a deteriorated IVD. (B) Therapeutic miRNAs are transmitted to degenerated IVD NP cells by MSC-derived exosomes, which hinder the translation process, regulating many intracellular processes such as apoptosis, pyroptosis, aging, ECM disintegration, and cytokine release. (C) IVD regeneration after MSC-derived exosome therapy, with increased cell proliferation, ECM production, and NP hydration, autophagy, decreased cytokines, and increased mitochondrial protein expression.

Figure 5 Therapeutic molecules (miRNAs) transferred by MSC-derived exosomes in treatment of IVDD. (A) Schematic representation of an experimental intradiscal injection of MSC-derived exosomes in a deteriorated IVD. (B) Therapeutic miRNAs are transmitted to degenerated IVD NP cells by MSC-derived exosomes, which hinder the translation process, regulating many intracellular processes such as apoptosis, pyroptosis, aging, ECM disintegration, and cytokine release. (C) IVD regeneration after MSC-derived exosome therapy, with increased cell proliferation, ECM production, and NP hydration, autophagy, decreased cytokines, and increased mitochondrial protein expression.