Review Article

Combining Nanotechnology and Gas Plasma as an Emerging Platform for Cancer Therapy: Mechanism and Therapeutic Implication

Table 2

Studies on combining nanoparticle and gas plasma treatment in vitro and in vivo.

Particle and gas plasma typeMain findingTumor entityRef.

AuNPs and helium-based plasma jet(i) Enhancement of the intracellular formation of superoxide andhydroxyl radical
(ii) Decrease in intracellular glutathione
(iii) Increase early apoptosis and secondary necrosis
(iv) Caused a significant increase in the sub-G1 fraction
(v) Reduction in G2/M levels
(vi) FAS externalization and caspase-8 activation
Melanoma[163]

AuNPs and plasma jet(i) Increase of cell death
(ii) Production of ROS/RNS
(iii) decrease of cancer cells viability
Glioblastoma[154]

Anti-NEU AuNPs and surface type air plasma(i) Reduction of proliferation rate
(ii) Increase of selective cancer cell death
Melanoma[164]

PEG-coated AuNPs and surface DBD air plasma(i) Decrease cancer cells viability
(ii) Inhibiting tumor cell proliferation
(iii) ROS/RNS-mediated apoptosis
(iv) Activation of tumor suppressors
(v) Inhibition of tumor growth
(vi) Reduction of migration and invasion in cancer cells
(vii) Decrease of tumor volume
(viii) Increase of E-cadherin in treated tissues
Glioblastoma[159]

AuNPs and DBD plasma(i) Augmentation of anti-cancer cytotoxicity
(ii) Increasing AuNP endocytosis and trafficking to lysosomes in cancer cells
(iii) Enhancement of AuNP uptake
Glioblastoma[160]

AuNPs and plasma jet(i) Decrease of cell viability
(ii) Improvement of NPs uptake rate into cells
(iii) Increment of ROS/RNS intensity in the cancer cells
Glioblastoma[161]

FAK antibody conjugated-AuNPs and DBD plasma(i) Inhibition of the viability of cancer cells
(ii) Induction of apoptosis
(iii) Decrease of cell cycle phase in G1
(iv) Increase of the number of apoptotic cells
Melanoma[165]

Fluorouracil loaded PLGA NPs and plasma jet(i) Induction of cytotoxic effects
(ii) Decrease of metastatic gene expression
(iii) Enhancement of anti-cancer effects
(iv) Exhibited anti-proliferative effects
(v) Increase of cellular internalization of NPs
Breast cancer[149]

Iron NPs and plasma jet(i) Reduction in cell proliferation
(ii) Induction apoptotic process
(iii) Showed DNA fragmentation
(iv) Increment of cancer cell death
Breast cancer[168]

Epidermal growth factor conjugated AuNPs and DBD plasma(i) Increase in cytotoxicity
(ii) Enhancement of the apoptotic response
Lung cancer[249]

Silica, silver, iron oxide, cerium oxide, titanium oxide, and iron-doped titanium oxide NPs, and plasma jet(i) Reduction of growth pattern
(ii) Increased cytotoxic effects
(iii) ROS/RNS generation
Melanoma[166]

AuNPs and plasma jet(i) Increase of apoptotic cell death
(ii) Induction of nuclear condensation and DNA fragmentation
Colorectal cancer[250]
Iron oxide-based magnetic NPs and plasma jet(i) Decrease of cell viability
(ii) Indication of high levels of ROS/RNS
(iii) G0/G1 Phase cell cycle arrest and condensation of nuclei
(iv) Inhibitory effect on cell migration and invasion
(v) Indicating intensive necrosis and apoptosis
(vi) Inhibition of cancer cells proliferation
(vii) Restraining tumor growth and reduction of tumor size
Lung cancer[169]

PLGA-magnetic iron oxide NPs and plasma jet(i) Inhibition of cancer cells proliferation
(ii) Enhancement of cytotoxicity
(iii) Induction of necrosis and apoptosis
(iv) Increase of intracellular ROS/RNS levels
Lung cancer[142]

Production of AuNPs by gas plasma(i) Reduction of invasive cancer cell proliferation
(ii) Induction of cancer cell apoptosis
(iii) Impairment of cell migration
Breast cancer[251]

Platinum NPs and plasma jet(i) Decrease in the viability of cancer cells
(ii) Enhancement the percentage of apoptosis cells
(iii) Increment in the percentage of DNA fragmentation
(iv) Decrease of cells in the G1 cell cycle phases
(v) Induction of ROS/RNS production
(vi) Augment of intracellular Ca2+ levels
Lymphoma[252]

AuNPs and gas plasma(i) Gas plasma-stimulated AuNP uptake
(ii) Constant production of ROS/RNS (especially H2O2, NO2-, and NO3-)
(iii) Gas plasma-induced lipid peroxidation
(iv) Increase of AuNPs uptake through endocytosis
Glioblastoma[162]

Anti-EGFR-AuNPs and air plasma(i) Increment of death rate and proliferation
(ii) Increase necrosis
Melanoma and oral cancer[167]

PEG-AuNPs and plasma jet(i) Production of singlet oxygen
(ii) Hot electrons cause gold−PEG bond
[253]

Curcumin loaded on triphosphate chitosan NPs by plasma jet(i) Decrease of cell viability
(ii) Induction of sub-G1; arrest of G2/M
(iii) Upregulation of TP53 mRNA expression as a tumor suppressor
(iv) Increase in the percentage of apoptotic cells
Breast cancer[254]