Skip to main content

Table 3 Summary on the preparation and therapeutic activity of various BP-based preparations for postoperative treatment of tumors in solid tissues

From: Black phosphorous nanomaterials as a new paradigm for postoperative tumor treatment regimens

Carrier substrate

Therapeutic additive

Tumor indication

Antitumor mechanism

Wound healing mechanism

Refs.

PDLLA-PEG‐PDLLA: PLEL hydrogel

No

Resected HeLa tumors

PTT

PTT-mediated antibacterial effect

[83]

Gelatin hydrogels

No

Resected breast cancer

PTT

PTT-enhanced formation of lipid droplets and adipogenic related genes, hydrogel facilitated migration and infiltration of normal cells

[84]

Agarose hydrogel

Stress granule inhibitor Emetine

Hepatocellular carcinoma

Emetine suppresses stress granule formation to sensitize tumors for PTT

Not mentioned

[85]

Cellulose hydrogel

No

Melanoma, hepato-carcinoma and reticulum cell sarcoma

PTT

Not mentioned

[86]

Agarose hydrogel

Doxorubicin

Breast cancer, cervical cancer, lung carcinoma, melanoma

PTT, PTT-triggered drug release

Not mentioned

[87]

Gelatin-PCL nanofibrous scaffold

Doxorubicin

Resected melanoma

PTT, PTT-triggered drug release

Release of phosphates and phosphonates, photothermal stimulation of ERK1/2 and PI3K/Akt healing pathways

[88]

BPs are first coated with tumor cell membrane then loaded into hyaluronic acid/pluronic F-127 hydrogels

PD-1 antibody, GM-CSF and lipopolysaccharide

Triple negative breast cancer

PTT-stimulated cross-presentation by APCs and PTT-triggered aPD-1 release

Not mentioned

[89]

NIPAM hydrogel

γδ T cell agonist zoledronate

Breast cancer, bladder cancer

PTT, PTT-triggered zoledronate release

Not mentioned

[90]

PPS-PAA-PEG vesicle

Ag+ions

Triple negative breast cancer

PDT, PDT/Ag+ stimulated antitumor immune responses

Ag+-mediated antibacterial effects

[96]