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2.
Sci Rep ; 11(1): 8475, 2021 04 19.
Article in English | MEDLINE | ID: mdl-33875781

ABSTRACT

Microwave (MW) radiation is increasingly being used for several biological applications. Many investigations have focused on understanding the potential influences of pulsed MW irradiation on biological solutions. The current study aimed to investigate the effects of 3.5 GHz pulsed MW radiation-irradiated liquid solutions on the survival of human cancer and normal cells. Different physiological solutions such as phosphate buffer saline, deionized water, and Dulbecco's modified Eagle medium (DMEM) for cell culture growth were irradiated with pulsed MW radiation (45 shots with the energy of 1 mJ/shot). We then evaluated physiological effects such as cell viability, metabolic activity, mitochondrial membrane potential, cell cycle, and cell death in cells treated with MW-irradiated biological solutions. As MW irradiation with power density ~ 12 kW/cm2 mainly induces reactive nitrogen oxygen species in deionized water, it altered the cell cycle, membrane potential, and cell death rates in U373MG cells due to its high electric field ~ 11 kV/cm in water. Interestingly, MW-irradiated cell culture medium and phosphate-buffered saline did not alter the cellular viability and metabolic energy of cancer and normal cells without affecting the expression of genes responsible for cell death. Taken together, MW-irradiated water can alter cellular physiology noticeably, whereas irradiated media and buffered saline solutions induce negligible or irrelevant changes that do not affect cellular health.


Subject(s)
Biomarkers, Tumor/metabolism , Brain Neoplasms/pathology , Gene Expression Regulation, Neoplastic/radiation effects , Microwaves/therapeutic use , Nitric Oxide/metabolism , Apoptosis , Biomarkers, Tumor/genetics , Brain Neoplasms/genetics , Brain Neoplasms/metabolism , Brain Neoplasms/radiotherapy , Cell Cycle , Cell Proliferation , Glioma , Humans , Tumor Cells, Cultured
3.
Pharmaceutics ; 11(12)2019 Dec 14.
Article in English | MEDLINE | ID: mdl-31847372

ABSTRACT

Nucleic acid-based adjuvants have recently emerged as promising candidates for use in cancer vaccines to induce tumor-suppressing immune cells. In this study, we tested whether complexation of a nucleic acid-based adjuvant with chitosan (CTS) modulates immune adjuvant functions. As a nucleic acid-based adjuvant, we used toll-like receptor 3-recognizing RNA adjuvant (RA). Negatively charged RA formed nanoscale polyplexes with cationic CTS that possessed positive zeta potentials. RA/CTS polyplexes exerted dendritic cell (DC)-maturation effects without causing significant DC toxicity. This DC-maturation effect was CTS molecular weight dependent, with RA/CTS polyplexes with a CTS molecular weight of 340 kDa (RA/CTS 340K) producing the greatest effect. Subcutaneous injection of RA/CTS 340K polyplexes with the model tumor antigen ovalbumin exerted a preventive effect against challenge by ovalbumin-expressing tumor cells. It also provided greater inhibitory effects against a second challenge with the same tumor cells compared with other treatments. These protective effects of subcutaneous RA/CTS polyplex treatment were associated with the highest tumor antigen-specific humoral and cellular immune responses after tumor challenge, and with the greatest infiltration of CD4 helper T cell and CD8 T cell into the tumor tissues. Mice vaccinated with ovalbumin and RA/CTS polyplexes showed complete survival, even after repeated challenge with tumor cells. Our results suggest the potential of RA/CTS polyplexes as effective nanoadjuvants in the design of tumor vaccines and cancer immunotherapy.

4.
ACS Nano ; 13(7): 7442-7462, 2019 07 23.
Article in English | MEDLINE | ID: mdl-31180642

ABSTRACT

Although immune checkpoint inhibitors have emerged as a breakthrough in cancer therapy, a monotherapy approach is not sufficient. Here, we report an immune checkpoint inhibitor-modified nanoparticle for an in situ-assembled tumor vaccine that can activate immune systems in the tumor microenvironment and prevent the long-term recurrence of tumors. Adjuvant-loaded nanoparticles were prepared by entrapping imiquimod (IQ) in photoresponsive polydopamine nanoparticles (IQ/PNs). The surfaces of IQ/PNs were then modified with anti-PDL1 antibody (PDL1Ab-IQ/PNs) for in situ assembly with inactivated tumor cells and immune checkpoint blocking of PDL1 (programmed cell death 1 ligand 1). The presence of anti-PDL1 antibodies on IQ/PNs increased the binding of nanoparticles to CT26 cancer cells overexpressing PDL1. Subsequent near-infrared (NIR) irradiation induced a greater photothermal anticancer effect against cells treated with PDL1Ab-IQ/PNs than cells treated with plain PNs or unmodified IQ/PNs. To mimic the tumor microenvironment, we cocultured bone marrow-derived dendritic cells with CT26 cells treated with various nanoparticle formulations and NIR irradiated. This coculture study revealed that NIR-inactivated, PDL1Ab-IQ/PN-bound CT26 cells induced maturation of dendritic cells to the greatest extent. Following a single intravenous administration of different nanoparticle formulations in CT26 tumor-bearing mice, PDL1Ab-IQ/PNs showed greater tumor tissue accumulation than unmodified nanoparticles. Subsequent NIR irradiation of mice treated with PDL1Ab-IQ/PNs resulted in tumor ablation. In addition to primary tumor ablation, PDL1Ab-IQ/PNs completely prevented the growth of a secondarily challenged CT26 tumor at a distant site, producing 100% survival for up to 150 days. A long-term protection study revealed that treatment with PDL1Ab-IQ/PNs followed by NIR irradiation inhibited the growth of distant, secondarily challenged CT26 tumors 150 days after the first tumor inoculation. Moreover, increased infiltration of T cells was observed in tumor tissues treated with PDL1Ab-IQ/PNs and NIR-irradiated, and T cells isolated from splenocytes of mice in which tumor recurrence was prevented showed active killing of CT26 cells. These results suggest that PDL1Ab-IQ/PNs in conjunction with NIR irradiation induce a potent, in situ-assembled, all-in-one tumor vaccine with adjuvant-containing nanoparticle-bound, inactivated tumor cells. Such in situ nanoadjuvant-assembled tumor vaccines can be further developed for long-term prevention of tumor recurrence without the need for chemotherapy.


Subject(s)
Adjuvants, Immunologic , Cancer Vaccines/immunology , Colorectal Neoplasms/prevention & control , Nanoparticles/chemistry , Neoplasm Recurrence, Local/prevention & control , Animals , Cancer Vaccines/administration & dosage , Cancer Vaccines/chemistry , Colorectal Neoplasms/immunology , Dendritic Cells/immunology , Female , Mice , Mice, Inbred BALB C , Nanoparticles/administration & dosage , Neoplasm Recurrence, Local/immunology , Tumor Cells, Cultured
5.
Sci Rep ; 7(1): 8395, 2017 08 21.
Article in English | MEDLINE | ID: mdl-28827766

ABSTRACT

Although various oral pathogens are inactivated by non-thermal atmospheric pressure plasma (NTAPP), the in vivo effects of NTAPP are poorly understood. The first aim of this study was to examine the antibacterial activity of microwave-pulsed NTAPP against Staphylococcus aureus in artificial saliva to mimic oral environmental conditions. The second aim was to determine the influence of microwave-pulsed NTAPP on human gingival fibroblasts (HGFs). The microwave-pulsed NTAPP reduced bacterial viability (as measured by colony forming units [CFU]) to a greater extent in artificial saliva than in saline. Extending the post-treatment incubation time increased bacterial inactivation in artificial saliva compared to saline. HGFs viability was unaffected by microwave-pulsed NTAPP for bacterial inactivation. Rather, HGFs proliferation increased after a 5-min microwave-pulsed NTAPP. Less tumor necrosis factor alpha was released by microwave-pulsed NTAPP-treated HGFs stimulated with lipopolysaccharide (LPS) than by untreated, LPS-stimulated HGFs; thus, plasma appeared to suppress the inflammatory response. Our study suggests that microwave-pulsed NTAPP may have stronger in vivo antibacterial activity than in vitro activity, and that microwave-pulsed NTAPP may have the additional advantage of suppressing gingival inflammatory responses.


Subject(s)
Disinfectants/pharmacology , Microwaves , Mouth/microbiology , Plasma Gases/pharmacology , Staphylococcus aureus/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Cells, Cultured , Colony Count, Microbial , Fibroblasts/drug effects , Humans , Microbial Viability/drug effects , Models, Biological , Saliva, Artificial
6.
J Food Sci ; 80(5): M1031-8, 2015 May.
Article in English | MEDLINE | ID: mdl-25847522

ABSTRACT

The biochemistry and microbial ecology of 2 similar types of watery (mul) kimchi, containing sliced and unsliced radish and vegetables (nabak and dongchimi, respectively), were investigated. Samples from kimchi were fermented at 4, 10, and 20 °C were analyzed by plating on differential and selective media, high-performance liquid chromatography, and high-throughput DNA sequencing of 16S rDNA. Nabak kimchi showed similar trends as dongchimi, with increasing lactic and acetic acids and decreasing pH for each temperature, but differences in microbiota were apparent. Interestingly, bacteria from the Proteobacterium phylum, including Enterobacteriaceae, decreased more rapidly during fermentation at 4 °C in nabak cabbage fermentations compared with dongchimi. Although changes for Proteobacterium and Enterobacteriaceae populations were similar during fermentation at 10 and 20 °C, the homolactic stage of fermentation did not develop for the 4 and 10 °C samples of both nabak and dongchimi during the experiment. These data show the differences in biochemistry and microbial ecology that can result from preparation method and fermentation conditions of the kimchi, which may impact safety (Enterobacteriaceae populations may include pathogenic bacteria) and quality (homolactic fermentation can be undesirable, if too much acid is produced) of the product. In addition, the data also illustrate the need for improved methods for identifying and differentiating closely related lactic acid bacteria species using high-throughput sequencing methods.


Subject(s)
DNA, Bacterial/isolation & purification , Fermentation , Food Microbiology , Vegetables/microbiology , DNA, Bacterial/chemistry , DNA, Bacterial/classification , DNA, Ribosomal/chemistry , Enterobacteriaceae/classification , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Lactobacillus/classification , Proteobacteria/classification , Proteobacteria/genetics , Proteobacteria/isolation & purification , RNA, Ribosomal, 16S/genetics , Raphanus/microbiology , Sequence Analysis, DNA , Temperature
7.
Rev Sci Instrum ; 82(1): 016106, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21280869

ABSTRACT

In this paper, a picosecond impulse generator using step recovery diodes (SRDs) is presented. In order to reduce the pulse width of an impulse generator, we employed a cascaded SRD pulse-shaping circuit. A short impulse generation is confirmed in numerical simulation of a time-transient circuit simulator. Measurements show that the measured pulse width of the cascaded SRD impulse generator is 250 ps at 10% of the peak amplitude, which is improved by 85 ps compared with a conventional SRD impulse generator.

8.
J Control Release ; 145(2): 159-64, 2010 Jul 14.
Article in English | MEDLINE | ID: mdl-20385182

ABSTRACT

For delivery of siRNA, chitosan (CS) was derivatized with poly-l-arginine (PLR) and polyethylene glycol (PEG). The formation of polyplexes with siRNA was confirmed by gel retardation. The PLR-grafted CS formed nanosized particles with siRNA. PLR-grafted CS showed higher cellular delivery efficiency of siRNA than did CS, pegylated CS, PLR, or pegylated PLR. The extent of reduction in the expression of fluorescent proteins was highest following treatment of the cells using PLR derivatives of CS in complexes with specific siRNAs. Cell viability was greater in populations treated with pegylated CS-PLR than in those treated with PLR. Hemolysis of erythrocytes was reduced upon conjugation of PLR with CS. The delivery of siRNAs via pegylated CS-PLR revealed little dependence on serum. Molecular imaging techniques revealed that the intratumoral administration of red fluorescent protein-specific siRNA in complexes with pegylated CS-PLR significantly silenced the expression of red fluorescent proteins in tumor tissues in vivo. These results indicate that pegylated CS-PLR might be useful for in vivo delivery of therapeutic siRNAs.


Subject(s)
Chitosan/chemistry , RNA, Small Interfering/administration & dosage , Animals , Arginine/chemistry , Carcinoma, Hepatocellular/pathology , Carcinoma, Hepatocellular/therapy , Cell Line, Tumor , Cell Survival/drug effects , Drug Carriers , Hemolysis/drug effects , Humans , Liver Neoplasms/pathology , Liver Neoplasms/therapy , Lung Neoplasms/pathology , Lung Neoplasms/therapy , Mice , Molecular Weight , Polyethylene Glycols/chemistry , Polymers/chemistry , Polymers/pharmacology , Polymers/toxicity
9.
J Nanosci Nanotechnol ; 8(9): 4761-6, 2008 Sep.
Article in English | MEDLINE | ID: mdl-19049103

ABSTRACT

We prepared organic sensitizers (S1 and S2) containing julolidine moiety as a donor, phenyl or phenylene thiophene units as a conjugation bridge, and cyano acetic acid as an acceptor for dye sensitized solar cells. S1 exhibited two absorption maxima at 441 nm (epsilon = 26,200) and 317 nm (epsilon = 15,500) due to the pi-pi transition of the dye molecule. S2 dyes with an additional thiophene unit showed the absorption maximum extended by 18 nm. DSSCs based on S1 dye achieved 2.66% of power conversion efficiency with 8.3 mA cm(-2) of short circuit current, 576 mV of open circuit voltage, and 0.56 of fill factor. DSSCs using S2 dye with a longer conjugation attained only 1.48% of power conversion efficiency. The 0.21 V lower driving force for regeneration of the S2 dye compared to the Si dye is one of the reasons for low conversion efficiency of the S2 dye.

10.
Rev Sci Instrum ; 78(10): 104703, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17979445

ABSTRACT

This article introduces a low-cost phase detection radar aimed at measuring the human heartbeat and respiration signals without any physical connections to the human body. A continuous-wave radar targeting the chest will detect the phase difference, resulted by the time-varying target position of the heartbeat, between the transmitted signal and the reflected signal. We have tested the developed radar to measure the heartbeat and respiration signals at a distance of about 40 cm from the chest.


Subject(s)
Diagnosis, Computer-Assisted/instrumentation , Diagnosis, Computer-Assisted/methods , Heart Function Tests/instrumentation , Heart Rate/physiology , Radar/instrumentation , Respiratory Function Tests/instrumentation , Respiratory Mechanics/physiology , Equipment Design , Equipment Failure Analysis , Humans , Reproducibility of Results , Respiratory Function Tests/methods , Sensitivity and Specificity
11.
Org Lett ; 7(2): 323-6, 2005 Jan 20.
Article in English | MEDLINE | ID: mdl-15646988

ABSTRACT

[Structure: see text] Anthracene derivatives with a variety of donor-acceptor substituents have been synthesized and shown to exhibit large two-photon cross sections over a wide range of wavelengths.


Subject(s)
Anthracenes/chemistry , Anthracenes/chemical synthesis , Fluorescence , Photons , Styrenes/chemistry , Styrenes/chemical synthesis , Amines/chemistry , Molecular Structure
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