Publications by authors named "Garanina A"

Article Synopsis
  • Neutrophils show potential for delivering nanodrugs to tumors, with this study focusing on how they internalize different types of nanoparticles, like liposomes and PLGA.
  • Various techniques were used, including microscopy and flow cytometry, to assess how well neutrophils take up these nanoparticles and how cultivation conditions affect this process.
  • Results indicated that while all nanoparticles were taken up, the mechanisms varied; notably, the presence of plasma and specific immunoglobulins were crucial for the internalization of PLGA nanoparticles, highlighting the role of the external environment in enhancing drug delivery efficacy.
View Article and Find Full Text PDF

Background: The centrosome is the main center of the organization of microtubules (MT) in the cell, the origin for the formation of flagella and cilia, as well as the site of many regulatory intracellular processes. In diploid cells, the centrosome includes two centrioles connected to some additional structures and surrounded by pericentriolar material.

Methods: The ultrastructure of the cells was studied using transmission electron microscopy on serial ultrathin sections.

View Article and Find Full Text PDF
Article Synopsis
  • The paper discusses a new nanopipette sensor designed to detect copper ions, which is important for diagnosing and treating diseases like cancer and Alzheimer's.
  • This sensor can measure copper levels in various biological contexts, including individual cancer cells, tumor spheroids, and the brains of transgenic mouse models.
  • The research highlights the sensor's enhanced stability, selectivity, and effectiveness, making it a valuable tool for studying copper metabolism and the effectiveness of copper-based drugs.
View Article and Find Full Text PDF

Insufficient drug accumulation in tumors is still a major concern for using cancer nanotherapeutics. Here, the neutrophil-based delivery of three nanoparticle types-liposomes, PLGA, and magnetite nanoparticles-was assessed both in vitro and in vivo. Confocal microscopy and a flow cytometry analysis demonstrated that all the studied nanoparticles interacted with neutrophils from the peripheral blood of mice with 4T1 mammary adenocarcinoma without a significant impact on neutrophil viability or activation state.

View Article and Find Full Text PDF

Prostate cancer is the second most common cancer among men. We designed and synthesized new ligands targeting prostate-specific membrane antigen and suitable for bimodal conjugates with diagnostic and therapeutic agents. studies of the affinity of the synthesized compounds to the protein target have been carried out.

View Article and Find Full Text PDF

In connection with the emergence of new pathogenic strains of , the search for more effective antifungal drugs becomes a challenge. Part of the preclinical trials of such drugs can be carried out using the innovative ion-conductance microscopy (ICM) method, whose unique characteristics make it possible to study the biophysical characteristics of biological objects with high accuracy and low invasiveness. We conducted a study of a novel synthesized thiazolidinedione's antimicrobial (for spp.

View Article and Find Full Text PDF

We report herein the design, synthesis, and biological investigation of a series of novel Pt(IV) prodrugs with non-steroidal anti-inflammatory drugs naproxen, diclofenac, and flurbiprofen, as well as these with stearic acid in the axial position. Six Pt(IV) prodrugs were designed, which showed superior antiproliferative activity compared to cisplatin as well as an ability to overcome tumor cell line resistance to cisplatin. By tuning the drug lipophilicity via variation of the axial ligands, the most potent Pt(IV) prodrug was obtained, with an enhanced cellular accumulation of up to 153-fold that of cisplatin and nanomolar cytotoxicity both in 2D and 3D cell cultures.

View Article and Find Full Text PDF

The biodistribution of chemotherapy compounds within tumor tissue is one of the main challenges in the development of antineoplastic drugs, and techniques for simple, inexpensive, sensitive, and selective detection of various analytes in tumors are of great importance. In this paper we propose the use of platinized carbon nanoelectrodes (PtNEs) for the electrochemical detection of platinum-based drugs in various biological models, including single cells and tumor spheroids and inside solid tumors . We have demonstrated the quantitative direct detection of Pt(II) in breast adenocarcinoma MCF-7 cells treated with cisplatin and a cisplatin-based DNP prodrug.

View Article and Find Full Text PDF

Magnetic nanoparticles (MNPs) are widely considered for cancer treatment, in particular for magnetic hyperthermia (MHT). Thereby, MNPs are still being optimized for lowest possible toxicity on organisms while the magnetic properties are matched for best heating capabilities. In this study, the biocompatibility of 12 nm cobalt ferrite MNPs, functionalized with citrate ions, in different dosages on mice and rats of both sexes was investigated for 30 days after intraperitoneal injection.

View Article and Find Full Text PDF

This work is devoted to studying the effects of non-magnetic shell coating on nanoparticles in a low frequency alternating magnetic field (LF AMF) on tumor cells in vitro. Two types of iron oxide nanoparticles with the same magnetic core with and without silica shells were synthesized. Nanoparticles with silica shells significantly decreased the viability of PC3 cancer cells in a low frequency alternating magnetic field according to the cytotoxicity test, unlike uncoated nanoparticles.

View Article and Find Full Text PDF

Solid solution AuFe nanoparticles were synthesized for the first time under ambient conditions by an adapted method previously established for the FeO-Au core-shell morphology. These AuFe particles preserved the fcc structure of Au incorporated with paramagnetic Fe atoms. The metastable AuFe can be segregated by transformation into Janus Au/Fe particles with bcc Fe and fcc Au upon annealing.

View Article and Find Full Text PDF

Prostate-specific membrane antigen (PSMA), also known as glutamate carboxypeptidase II (GCPII), is a suitable target for specific delivery of antitumor drugs and diagnostic agents due to its overexpression in prostate cancer cells. In the current work, we describe the design, synthesis, and biological evaluation of novel low-molecular PSMA ligands and conjugates with fluorescent dyes FAM-5, SulfoCy5, and SulfoCy7. evaluation of synthesized PSMA ligands on the activity of PSMA shows that the addition of aromatic amino acids into a linker structure leads to a significant increase in inhibition.

View Article and Find Full Text PDF

The application of cell carriers for transporting nanodrugs to the tumor draws much attention as the alternative to the passive drug delivery. In this concept, the neutrophil (NΦ) is of special interest as this cell is able to uptake nanoparticles (NPs) and cross the vascular barrier in response to tumor signaling. There is a growing body of literature describing NP-NΦ interactions in vitro and in vivo that demonstrates the opportunity of using these cells to improve the efficacy of cancer therapy.

View Article and Find Full Text PDF
Article Synopsis
  • There is significant variability in how much liposomal drugs accumulate in human tumors, affecting their treatment response, making it crucial to determine patient eligibility for therapies.* -
  • The study utilizes in vivo imaging to confirm that magnetic liposomes (ML) can effectively predict tumor response to nanomedicine therapy without being influenced by prior doses of liposomes.* -
  • Results show that higher accumulation of ML in tumors leads to reduced tumor size and improved survival rates when combined with liposomal doxorubicin, highlighting the need for effective imaging techniques to enhance cancer treatment outcomes.*
View Article and Find Full Text PDF

A strategy for stereoselective synthesis of molecular platform for targeted delivery of bimodal therapeutic or theranostic agents to the prostate-specific membrane antigen (PSMA) receptor was developed. The proposed platform contains a urea-based, PSMA-targeting Glu-Urea-Lys (EuK) fragment as a vector moiety and tripeptide linker with terminal amide and azide groups for subsequent addition of two different therapeutic and diagnostic agents. The optimal method for this molecular platform synthesis includes (a) solid-phase assembly of the polypeptide linker, (b) coupling of this linker with the vector fragment, (c) attachment of 3-aminopropylazide, and (d) amide and carboxylic groups deprotection.

View Article and Find Full Text PDF

Heterodimeric nanoparticles comprising materials with different functionalities are of great interest for fundamental research and biomedical/industrial applications. In this work, FeO-Au nano-heterostructures were synthesized by a one-step thermal decomposition method. The hybrid nanoparticles comprise a highly crystalline 12 nm magnetite octahedron decorated with a single noble metal sphere of 6 nm diameter.

View Article and Find Full Text PDF

monitoring of reactive oxygen species (ROS) in tumors during treatment with anticancer therapy is important for understanding the mechanism of action and in the design of new anticancer drugs. In this work, a platinized nanoelectrode is placed into a single cell for detection of the ROS signal, and drug-induced ROS production is then recorded. The main advantages of this method are the short incubation time with the drug and its high sensitivity which allows the detection of low intracellular ROS concentrations.

View Article and Find Full Text PDF

Since the asialoglycoprotein receptor (also known as the "Ashwell-Morell receptor" or ASGPR) was discovered as the first cellular mammalian lectin, numerous drug delivery systems have been developed and several gene delivery systems associated with multivalent ligands for liver disease targeting are undergoing clinical trials. The success of these systems has facilitated the further study of new ligands with comparable or higher affinity and less synthetic complexity. Herein, we designed two novel trivalent ligands based on the esterification of tris(hydroxymethyl) aminomethane (TRIS) followed by the azide-alkyne Huisgen cycloaddition with azido -acetyl-d-galactosamine.

View Article and Find Full Text PDF

Magnetic hyperthermia (MHT) is a promising approach for cancer therapy. However, a systematic MHT characterization as function of temperature on the therapeutic efficiency is barely analyzed. Here, we first perform comparative temperature-dependent analysis of the cobalt ferrite nanoparticles-mediated MHT effectiveness in two murine tumors models - breast (4T1) and colon (CT26) cancer in vitro and in vivo.

View Article and Find Full Text PDF

Recently neutrophil-based nanoparticles (NPs) drug delivery systems have gained considerable attention in cancer therapy. Numerous studies have been conducted to identify optimal NPs parameters for passive tumor targeting, while there is a fundamental dearth of knowledge about the factors governing cell-mediated delivery. Here, by using intravital microscopy and magnetic resonance imaging, we describe accumulation dynamics of 140 nm magnetic cubes and clusters in murine breast cancer (4T1) and colon cancer (CT26) models.

View Article and Find Full Text PDF

High polyspermy is one of the major limitations of porcine invitro fertilisation (IVF). The addition of oviductal fluid (OF) during IVF reduces polyspermy without decreasing the fertilisation rate. Because extracellular vesicles (EVs) have been described as important OF components, the aim of this study was to evaluate the effect of porcine oviductal EVs (poEVs) on IVF efficiency compared with porcine OF (fresh and lyophilised).

View Article and Find Full Text PDF
Article Synopsis
  • Liposomes are widely used as nanocarriers for cancer treatment, but there are still challenges related to their delivery efficiency and unwanted accumulation in healthy tissues.
  • Research using intravital microscopy on different tumor models revealed two distinct patterns of liposome leakage: microleakage, which deposits nanoparticles near blood vessels without reaching tumor cells, and macroleakage, which allows deeper penetration into tumors.
  • Neutrophils play a key role in triggering these leakages, affecting the delivery of liposomes; understanding these mechanisms could enhance the design of more effective nanodrugs for cancer therapy.
View Article and Find Full Text PDF

Despite the progress of modern medicine, oncological diseases are still among the most common causes of death of adult populations in developed countries. The current therapeutic approaches are imperfect, and the high mortality of oncological patients under treatment, the lack of personalized strategies, and severe side effects arising as a result of treatment force seeking new approaches to therapy of malignant tumors. During the last decade, cancer immunotherapy, an approach that relies on activation of the host antitumor immune response, has been actively developing.

View Article and Find Full Text PDF
Article Synopsis
  • Developing effective nanocarriers for targeted organ delivery and safe elimination is complex, particularly due to factors like size and composition influencing biodistribution.
  • Recent studies indicate that nanoparticles larger than the traditional renal clearance threshold can still be expelled through urine, challenging previous beliefs about the limits of nanoparticle size in excretion.
  • Research using advanced imaging techniques showed that PEGylated iron oxide nanoparticles accumulate quickly in the kidneys and can be excreted intact, suggesting a new pathway for renal clearance beyond the conventional glomerular filtration limits.
View Article and Find Full Text PDF

Intravital microscopy is widely used for in vivo studies of the mechanisms of carcinogenesis and response to antitumor therapy. For visualization of tumor cells in vivo, cell lines expressing fluorescent proteins are needed. Expression of exogenous proteins can affect cell growth rate and their tumorigenic potential.

View Article and Find Full Text PDF