Samah Shanwar

Mrs. Samah Shanwar

Institute of Biology and Biomedicine, Lobachevsky State University of Nizhny Novgorod
orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 September 2020 in Molecules
Verified
Journal Article
Open access
PDF file
EGEvgenii Guryev
Evgenii Guryev
ASAnita Smyshlyaeva
Anita Smyshlyaeva
Natalia ShilyaginaNatalia Shilyagina
Natalia Shilyagina
EVEvgeniya Voronova
Evgeniya Voronova
SSSamah Shanwar
Samah Shanwar
Andrei ZvyaginAndrei Zvyagin
Andrei Zvyagin
Theranostic approach is currently among the fastest growing trends in cancer treatment. It implies the creation of multifunctional agents for simultaneous precise diagnosis and targeted impact on tumor cells. A new type of theranostic complexes was created based on NaYF4: Yb,Tm upconversion nanoparticles coated with polyethylene glycol and functionalized with the HER2-specific recombinant targeted toxin DARPin-LoPE. The obtained agents bind to HER2-overexpressing human breast adenocarcinoma cells and demonstrate selective cytotoxicity against this type of cancer cells. Using fluorescent human breast adenocarcinoma xenograft models, the possibility of intravital visualization of the UCNP-based complexes biodistribution and accumulation in tumor was demonstrated.

28 March 2021 in Materials
Verified
Journal Article
Open access
PDF file
SSSamah Shanwar
Samah Shanwar
LLLiuen (Olivia) Liang
Liuen (Olivia) Liang
ANAndrey V. Nechaev
Andrey V. Nechaev
DBDaria K. Bausheva
Daria K. Bausheva
Irina V. BalalaevaIrina V. Balalaeva
Irina V. Balalaeva
EGEvgenii Guryev
Evgenii Guryev
In the natural fluidic environment of a biological system, nanoparticles swiftly adsorb plasma proteins on their surface forming a “protein corona”, which profoundly and often adversely affects their residence in the systemic circulation in vivo and their interaction with cells in vitro. It has been recognized that preformation of a protein corona under controlled conditions ameliorates the protein corona effects, including colloidal stability in serum solutions. We report on the investigation of the stabilizing effects of a denatured bovine serum albumin (dBSA) protein corona formed on the surface of upconversion nanoparticles (UCNPs). UCNPs were chosen as a nanoparticle model due to their unique photoluminescent properties suitable for background-free biological imaging and sensing. UCNP surface was modified with nitrosonium tetrafluoroborate (NOBF4) to render it hydrophilic. UCNP-NOBF4 nanoparticles were incubated in dBSA solution to form a dBSA corona followed up by lyophilization. As produced dBSA-UCNP-NOBF4 demonstrated high photoluminescence brightness, sustained colloidal stability after long-term storage and the reduced level of serum protein surface adsorption. These results show promise of dBSA-based nanoparticle pretreatment to improve the amiability to biological environments towards theranostic applications.

1 March 2020 in Doklady Biochemistry and Biophysics
Verified
Journal Article
Closed access
PDF file
EGE. L. Guryev
E. L. Guryev
ASA. S. Smyshlyaeva
A. S. Smyshlyaeva
NSN. Yu. Shilyagina
N. Yu. Shilyagina
SSSamah Shanwar
Samah Shanwar
AKA. B. Kostyuk
A. B. Kostyuk
RPR. V. Petrov
R. V. Petrov
Combining diagnostic and therapeutic functions in one agent is a promising strategy in the development of personalized approaches to the treatment of cancer. The opportunity to combine diagnostics and therapy appeared with the development of nanobiotechnologies and was realized in the concept of theranostics. To date, a number of promising agents based on nanomaterials capable of diagnosing, targeted therapeutic effects, and monitoring the response of tumor cells were obtained within the approach of theranostics. In this work, a new type of theranostic complexes based on upconversion nanoparticles coated with polyethylene glycol and functionalized with the DARPin–LoPE recombinant targeted toxin was developed. Selective binding of complexes to human breast adenocarcinoma cells overexpressing the HER2 receptor and specific toxicity to them were shown.