TY - JOUR
T1 - Antibody-Conjugated Gel-Coated Single-Walled Carbon Nanotubes as Photothermal Agents
AU - Nagai, Yukiko
AU - Nakamura, Kenta
AU - Ohno, Jun
AU - Kawaguchi, Minoru
AU - Fujigaya, Tsuyohiko
N1 - Funding Information:
We thank to prof. Masaru Tanaka for his supports of the cell experiments using NIH/3T3. This study was supported in part by the Nanotechnology Platform Project, Ministry of Education, Culture, Sports, Science, and Technology, Japan, KAKENHI (No. JP18H01816), the Japan Society for the Promotion of Science (JSPS), JSPS Bilateral Program (No. AJ190078), Grant-in-Aid for JSPS Fellows (No. 20J12870), and CREST (No. AJ199002) from JST, Japan.
Funding Information:
The mouse melanoma cell line, B16F10 (RCB2630), was provided by Fukuoka Dental College, through the RIKEN BRC, through the National Bio-Resource Project of the Ministry of Education, Culture, Sports and Technology (Ibaraki, Japan). Cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM; Wako Pure Chemical Industries, Ltd., Japan) supplemented with 10 wt % fetal calf serum (FBS) and 1 wt % Gibco Antibiotic-Antimycotic. Cells were cultured in vitro (37 °C, 5% CO) until confluent and were then detached using 0.25% trypsin/0.02% ethylenediaminetetraacetic acid (EDTA) solution. The detached cells were then used for the active cancer cell targeting and PTT assay. NIH/3T3 cells were provided by Kyushu university, through the Japanese Collection of Research Bioresources Cell Bank (JCRB Cell Bank, Osaka, Japan). Cells were maintained in DMEM (Thermo Fisher Scientific, Waltham, MA, U.S.A.) supplemented with 10 wt % FBS and 1 wt % penicillin-streptomycin (Thermo Fisher Scientific, Waltham, MA, U.S.A.). Cells were cultured in vitro (37 °C, 5% CO) until confluent and were then detached using 0.25% trypsin/0.02% EDTA solution. 2 2
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/6/21
Y1 - 2021/6/21
N2 - Photothermal therapy (PTT) using near-infrared (NIR) light is an attractive treatment modality for cancer, in which photothermal agents absorb energy from photons and convert it into thermal energy to lead to cancer cell death. Among the various organic and inorganic materials, single-walled carbon nanotubes (SWCNTs) are promising candidates for NIR photothermal agents due to their strong absorption in this region as well as their high photothermal conversion efficiency. In the development of the SWCNT-based PTT materials, modifications of SWCNTs to offer a stable dispersion for biocompatibility as well as to target the tumor of choice while maintaining their NIR absorption have been required. While modification of SWCNTs through noncovalent methods can be achieved, these modifications can be easily reversed in the body. Contrarily, modifications through covalent attachments, while more desirable, may compromise the NIR absorption characteristics of the SWCNTs. Previously, we reported the development of a synthetic strategy to coat SWCNTs with a cross-linked polymer (i.e., a gel) through a process called CNT Micelle Polymerization and successfully introduced maleimide groups that allowed for postmodification through the ene-thiol reaction without deteriorating the NIR absorption. In this report, we postmodify thiol-containing antibodies (anti-TRP-1, a melanoma specific protein) using maleimide chemistry and find that the SWCNTs conjugated with anti-TRP-1 maintain the characteristic NIR absorption as SWCNTs with dispersion stability. It is estimated that 50 maleimide groups are incorporated in one SWCNT (ca. 280 nm long) and they are modified with 32 TRP-1 fragments. Finally, we successfully use these targeted SWCNTs for the PTT of the melanoma cell line using NIR light (1064 nm; 2 W, 5 min). Our method can be extended to a vast array of specific antibodies as well as other targeting agents.
AB - Photothermal therapy (PTT) using near-infrared (NIR) light is an attractive treatment modality for cancer, in which photothermal agents absorb energy from photons and convert it into thermal energy to lead to cancer cell death. Among the various organic and inorganic materials, single-walled carbon nanotubes (SWCNTs) are promising candidates for NIR photothermal agents due to their strong absorption in this region as well as their high photothermal conversion efficiency. In the development of the SWCNT-based PTT materials, modifications of SWCNTs to offer a stable dispersion for biocompatibility as well as to target the tumor of choice while maintaining their NIR absorption have been required. While modification of SWCNTs through noncovalent methods can be achieved, these modifications can be easily reversed in the body. Contrarily, modifications through covalent attachments, while more desirable, may compromise the NIR absorption characteristics of the SWCNTs. Previously, we reported the development of a synthetic strategy to coat SWCNTs with a cross-linked polymer (i.e., a gel) through a process called CNT Micelle Polymerization and successfully introduced maleimide groups that allowed for postmodification through the ene-thiol reaction without deteriorating the NIR absorption. In this report, we postmodify thiol-containing antibodies (anti-TRP-1, a melanoma specific protein) using maleimide chemistry and find that the SWCNTs conjugated with anti-TRP-1 maintain the characteristic NIR absorption as SWCNTs with dispersion stability. It is estimated that 50 maleimide groups are incorporated in one SWCNT (ca. 280 nm long) and they are modified with 32 TRP-1 fragments. Finally, we successfully use these targeted SWCNTs for the PTT of the melanoma cell line using NIR light (1064 nm; 2 W, 5 min). Our method can be extended to a vast array of specific antibodies as well as other targeting agents.
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U2 - 10.1021/acsabm.1c00299
DO - 10.1021/acsabm.1c00299
M3 - Article
C2 - 35007053
AN - SCOPUS:85108629077
SN - 2576-6422
VL - 4
SP - 5049
EP - 5056
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 6
ER -