Bioproduced Nanoparticles Deliver Multiple Cargoes via Targeted Tumor Therapy In Vivo
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F24%3A00598904" target="_blank" >RIV/61388971:_____/24:00598904 - isvavai.cz</a>
Alternative codes found
RIV/86652036:_____/24:00598904 RIV/68081715:_____/24:00598904 RIV/46747885:24530/24:00013415
Result on the web
<a href="https://pubs.acs.org/doi/10.1021/acsomega.4c03277" target="_blank" >https://pubs.acs.org/doi/10.1021/acsomega.4c03277</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acsomega.4c03277" target="_blank" >10.1021/acsomega.4c03277</a>
Alternative languages
Result language
angličtina
Original language name
Bioproduced Nanoparticles Deliver Multiple Cargoes via Targeted Tumor Therapy In Vivo
Original language description
This study recognized biologically produced gold nanoparticles (AuNPs) as multiple cargo carriers with a perspective of drug delivery into specialized tumor cells in vivo. Paclitaxel (PTX), transferrin, and antimiR-135b were conjugated with AuNPs and their uptake by mouse tumor cells in an induced breast cancer model was investigated. Each of the above-mentioned molecules was conjugated to the AuNPs separately as well as simultaneously, loading efficiency of each cargo was assessed, and performance of the final product (FP) was judged. After tumor induction in BALB/c mice, sub-IC50 doses of FP as well as control AuNPs, PTX, and phosphate buffered saline were administered in vivo. Round AuNPs were prepared using Fusarium oxysporum and exhibited a size of 13 +/- 1.3 nm and a zeta potential of35.8 +/- 1.3 mV. The cytotoxicity of individual conjugates and FP were tested by MTT assay in breast tumor cells 4T1 and nontumor fibroblasts NIH/3T3 cells. The conjugation of individual molecules with AuNPs was confirmed, and FP (size of 54 +/- 14 nm and zeta potential of31.9 +/- 2.08 mV) showed higher 4T1-specific toxicity in vitro when compared to control conjugates. After in vivo application of the FP, transmission electron microscopy analyses proved the presence of AuNPs in the tumor cells. Hematoxylin and eosin staining of the tumor tissue revealed that the FP group exhibited the highest amounts of inflammatory, necrotic, and apoptotic cells in contrast to the control groups. Finally, qPCR results showed that FP could transfect and suppress miR-135b expression in vivo, confirming the tumor-targeting properties of FP. The capacity of biologically produced gold nanoparticles to conjugate with multiple decorative molecules while retaining their stability and effective intracellular uptake makes them a promising alternative strategy superior to current drug carriers.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10606 - Microbiology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
ACS Omega
ISSN
2470-1343
e-ISSN
2470-1343
Volume of the periodical
9
Issue of the periodical within the volume
31
Country of publishing house
US - UNITED STATES
Number of pages
16
Pages from-to
33789-33804
UT code for WoS article
001282225800001
EID of the result in the Scopus database
2-s2.0-85200879778