# Construction of Rough Surfaces Based on Zirconium Metal–Organic Frameworks to Enhance Photothermal and Photodynamic Therapy for Multiple Myeloma

**Authors:** Mengyu Xu, Lihua Ma, Min Liu, Yuanxin Chen, Xianjun Wang, Lijuan Wang, Yanxi Zhu

PMC · DOI: 10.34133/bmr.0330 · Biomaterials Research · 2026-02-20

## TL;DR

A new drug delivery system with a rough surface improves photothermal and photodynamic therapy for multiple myeloma by enhancing drug targeting and cell uptake.

## Contribution

A pH-responsive DDS with a rough surface constructed from zirconium MOFs is developed for enhanced tumor targeting and therapy.

## Key findings

- The system achieved a photothermal conversion efficiency of 26.8% with IR-820.
- The rough surface increased cell uptake and endocytosis in the acidic tumor microenvironment.
- HA-A6 polymer improved targeting via receptor-mediated recognition.

## Abstract

Nanotargeted drug delivery systems (nanotargeted DDS) have emerged as promising solutions to improve treatment precision and reduce toxicity. However, achieving efficient delivery from the bloodstream to the tumor site remains challenging due to the complex tumor microenvironment (TME). To address these issues, a novel pH-responsive surface-switching DDS, UiO@CeO2/IR@(bPEI/HA)-A6, was designed. This system features CeO2 immobilized on zirconium metal–organic frameworks (UiO-66-NH2) to create a rough surface, which is then further modified with bPEI and HA-A6 polymers, facilitating its transport in the blood. After loading the photosensitizer IR-820, its photothermal conversion efficiency reached 26.8%, enabling effective photothermal and photodynamic therapy. The HA-A6 polymer enhanced the targeting effect through receptor-mediated recognition, ensuring more drug accumulation at the tumor site; the rough surface constructed by CeO2 increased cell uptake and enhanced endocytosis in cells. The acidic TME exfoliates the coating, exposing the rough surface of CeO2, which marked enhances the cellular uptake of DDS, thereby laying a solid foundation for DDS to play an antitumor role. These results indicate that UiO@CeO2/IR@(bPEI/HA)-A6 has excellent potential in the treatment of multiple myeloma.

## Linked entities

- **Chemicals:** IR-820 (PubChem CID 16089390)
- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Genes:** ANXA5 (annexin A5) [NCBI Gene 308] {aka ANX5, CPB-I, ENX2, HEL-S-7, PP4, RPRGL3}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, BLNK (B cell linker) [NCBI Gene 29760] {aka AGM4, BASH, BLNK-S, LY57, SLP-65, SLP65}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, Cd44 (CD44 antigen) [NCBI Gene 12505] {aka HERMES, Ly-24, Pgp-1}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** hematological malignancy (MESH:D019337), necrosis (MESH:D009336), lymphoma (MESH:D008223), phototoxicity (MESH:D017484), DDS (MESH:D030321), Multiple Myeloma (MESH:D009101), Tumor (MESH:D009369), multiple (MESH:D009104), cytotoxicity (MESH:D064420), inflammation (MESH:D007249)
- **Chemicals:** MES (MESH:C004550), acetic acid (MESH:D019342), C6 (MESH:C517282), ethanol (MESH:D000431), DDS (MESH:C007792), A6 (MESH:C043832), UiO-66 (MESH:C000711576), ROS (MESH:D017382), HA (MESH:D006820), CCK-8 (MESH:D012844), water (MESH:D014867), CO2 (MESH:D002245), IR-820 (MESH:C541053), ZrCl4 (MESH:C429984), CeO2 (MESH:C030583), IR (MESH:D007495), DMF (MESH:D004126), MOFs (MESH:D000073396), CTAB (MESH:D000077286), polyelectrolytes (MESH:D000071228), streptomycin (MESH:D013307), polymer (MESH:D011108), indocyanine green (MESH:D007208), PI (MESH:D011419), calcein-AM (MESH:C085925), superoxide (MESH:D013481), silicon (MESH:D012825), (bPEI/HA) (-), paraffin (MESH:D010232), Zirconium Metal (MESH:D015040), H&amp;E (MESH:D006371), DHE (MESH:C067883), oxygen (MESH:D010100), penicillin (MESH:D010406), hematoxylin (MESH:D006416)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** F to H, C) for 24, C to E, F30 S
- **Cell lines:** UiO-66-NH2 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_9722), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), ARH-77 — Homo sapiens (Human), Transformed cell line (CVCL_1072), BPMI8226 — Homo sapiens (Human), Plasma cell myeloma, Cancer cell line (CVCL_0014), UiO@CeO2 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_A628)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921127/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921127/full.md

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Source: https://tomesphere.com/paper/PMC12921127