disadvantages of nanotechnology in cancer treatment disadvantages of nanotechnology in cancer treatment

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disadvantages of nanotechnology in cancer treatmentPor

May 20, 2023

Liposomes can be conjugated with poly(ethylene glycol) (PEG), targeting ligands and/or antibodies, polysaccharides on the external surface to enhance solubility, to increase the hydrophilicity and to provide passive and active targeting functions, in due course attaining high drug efficiency with low toxicity [233]. The fabricated nanoparticles enhanced cellular uptake via CD44 receptor-mediated endocytosis by HeLa cells. Cells were incubated for 48h and BCL-2 siRNA concentration used is 20nM (c); Mean tumor volume determined using magnetic resonance imaging measured after 25days of the first injection. Cells Nanomed. The site is secure. Adv. The use of diverse nanomaterials with desired properties and recent progress in the drug delivery arena have revealed outstanding challenges in cancer therapy and management. The in vivo antitumor studies were conducted on male BALB/C nude mice bearing a HepG2 tumor model. In spite of widespread research and the preclinical development of liposomal formulations from several decades, only a few liposomal drug formulations have been approved by the FDA for clinical use [246]. 12, 67876797 (2017), S.-B. 5(13), 16271637 (2016), F. Li et al., Near-infrared light stimuli-responsive synergistic therapy nanoplatforms based on the coordination of tellurium-containing block polymer and cisplatin for cancer treatment. Biomaterials 37, 447455 (2015), R. Chakravarty et al., Hollow mesoporous silica nanoparticles for tumor vasculature targeting and PET image-guided drug delivery. C 70, 763771 (2017), S. Bano et al., Smart nickel oxide based coreshell nanoparticles for combined chemo and photodynamic cancer therapy. Please enable it to take advantage of the complete set of features! Likewise, intracellular drug delivery can be enhanced by utilizing carbon nanotube-based phototherapies. Mater. Health B 14(8), 593632 (2011), H. Maeda, H. Nakamura, J. Fang, The EPR effect for macromolecular drug delivery to solid tumors: improvement of tumor uptake, lowering of systemic toxicity, and distinct tumor imaging in vivo. 2022 Mar 1;2(3):258-281. doi: 10.1021/acsbiomedchemau.2c00003. These surface modifiable mesoporous silica nanomaterials have been exploited to deliver curcumin to breast cancer cell lines that were loaded with hyaluronan or polyethyleneimine-folic acid and were tested on mouse xenograft model [221]. The advent of nanotechnology has revolutionized . is an important area in nanotechnology which refers to highly specific medical intervention at the molecular scale for diagnosis, prevention and treatment of diseases (11). Therefore, it is essential to consider how we can exploit the endoplasmic retention effects to achieve active targeting. Gao et al. 46, 11381148 (2018), H. Banu et al., Gold and silver nanoparticles biomimetically synthesized using date palm pollen extract-induce apoptosis and regulate p53 and Bcl-2 expression in human breast adenocarcinoma cells. 2023 Apr 4;28(1):28. doi: 10.1186/s11658-023-00442-z. Biopharm. Macromol. 12, 14531464 (2017), X. Hua et al., Magnetically triggered drug release from nanoparticles and its applications in anti-tumor treatment. Macromol. The cellular uptake of surface modified PLGA nanoparticles were in the order of vitamin E TPGS-coated PLGA>PVA-coated PLGA>naked PLGA nanoparticles [124]. 6, 286 (2015), B.S. Many such formulations have been approved [34], opening new avenues toward cancer therapeutics. Res. Mater. Control. et al. Macromol. Polymeric nanoparticles are colloidal nanoparticles wherein therapeutic molecules will be encapsulated or adsorbed or conjugated in the polymer matrix. Mol. Slowing, B.G. Usually, targeting based approaches exploit the subtle differences in the expression of substrate molecules between cancer and normal cells. Release 172(3), 852861 (2013), S.K. By using immunofluorescence labeling of an anti-Ki67 antibody, the Ki67-positive cells in tumor sections after two tail vein injections of 20mg/kg iron dose of IGF1-IONPs are measured. Daima, Nanomedicine in sensing, delivery, imaging and tissue engineering: advances, opportunities and challenges. Recently, nanotechnology and nanoparticles have attracted great interest in cancer therapeutics as they can provide improved and targeted drug delivery systems to overcome the drawbacks of conventional chemotherapy. Due to variable endothelial gaps resulting from vigorous tumorous cell growth, it can result in non-uniform extravasation of nanoparticles into the target area [36]. J. Pharm. -, The, L., LANCET, (2018) 392, 985. A review on dna nanobots - A new technique for cancer treatment Feazell et al., Soluble single-walled carbon nanotubes as longboat delivery systems for platinum(IV) anticancer drug design. Disclaimer. 30(45), 299315 (2009), Y. Kato et al., Acidic extracellular microenvironment and cancer. J. Nanomed. Likewise, PEG capped Au nanoparticles coated with [Pt(1R,2R-diaminocyclohexane) (H2O)2]2NO3 were takenup, and localized in the lung epithelial and colon cancer cell lines showing more significant effects than the drug alone [128]. Soc. A wide range of nanotherapeutics, composed of organic and inorganic nanomaterialshave been developed with multiple types of drugs or molecules for cancer imaging, detection and treatment. Adv. Drug Deliv. Manage cookies/Do not sell my data we use in the preference centre. Macromol. The https:// ensures that you are connecting to the Cancer is a disease with complex pathological process. Many anticancer drug applications are limited due to its solubility, stability, and bioavailability of the drug. Nanotechnology: A Promising Approach for Cancer Diagnosis, Therapeutic Pharm. Acad. J. 2023 Feb 26;13(5):876. doi: 10.3390/nano13050876. The chemical changes can also introduce changes in the hydrophobicity of the polymer, changing the integrity of nanoparticles and thereby leading to release of drug cargo. B 2(5), 452470 (2014), H. Alimoradi, et al., in Nanostructures for drug delivery. Interfaces 10, 2116021172 (2018), N. Guldris et al., Orthogonal clickable iron oxide nanoparticle platform for targeting, imaging, and on-demand release. Nanotechnology and Immunotherapy in Ovarian Cancer: Tracing - PubMed Interfaces 4(1), 466475 (2012), H. Yu et al., pH- and NIR light-responsive micelles with hyperthermia-triggered tumor penetration and cytoplasm drug release to reverse doxorubicin resistance in breast cancer. Biomed. Liu et al. J. Biol. To date, many types of organic nanocarriers have been developed such as liposomes, polymeric nanoparticles, dendrimers and micelles. Nanotechnology has the potential to facilitate the transport of drugs across the blood-brain barrier and to enhance their pharmacokinetic profile. Nanotechnology for early cancer detection. J. Nagraju, H.K. J. Pharm. Carbohyd. 394(1), 122142 (2010), R. Jevprasesphant et al., The influence of surface modification on the cytotoxicity of PAMAM dendrimers. Expert Opin. Bae, Drug targeting and tumor heterogeneity. In addition, many other factors have a profound consequence on nanomaterials uptake and distribution in cells. Healthc. 22(27), 1377313781 (2012), Y. Wang et al., Graphene oxide covalently grafted upconversion nanoparticles for combined NIR mediated imaging and photothermal/photodynamic cancer therapy. Initially, we mention different forms of ovarian cancer biomarkers involving CA125, human epididymis protein 4 (HE4), mucin 1 (MUC1), and prostate. Table2 highlights various inorganic nanocarriers for delivery of anticancer therapeutics. In another study, ultrasmall Au nanoparticles of sizes ranging from 2 to 15nm coated with tiopronin were evaluated for their localization and penetration into breast cancer cells, and it was found that accumulation of smaller nanoparticles was higher in tumor tissues in mice [104]. 5(10), 2104721054 (2018), L. Zhang, Y. Li, C.Y. To develop nanomaterials for specific biomedical applications, surface chemistry design is indispensable. Terms and Conditions, Similarly, the cellular uptake and in vivo fate of micellar nanoparticles have been explored, wherein negatively charged micellar nanoparticles were taken up by tumor cells, and the mechanism of internalization was determined to occur through multiple distinct endocytic pathways including clathrin-mediated endocytosis, caveolae-mediated endocytosis, and macropinocytosis. Recently, a hybrid material based on graphene oxide (GO) coated with -cyclodextrin (CD) and poly(amido amine) dendrimer (DEN) was used to deliver doxorubicin, camptothecin (CPT) and a photosensitizer (protoporphyrin IX (PpIX)). 112(5), 27392779 (2012), D. Peer et al., Nanocarriers as an emerging platform for cancer therapy. Am. Nat. Mater. Pharm. Such clinical trials are projected to intensify the use of polymeric drug delivery systems in the near future. For example, epidermal growth factor receptor (EGFR, responsible for epithelial tissue development and homeostasis) is overexpressed in cancerous cells relative to normal cells, as cancer cells grow and divide vigorously [50]. The targeted nanosystem established higher tumor inhibition and prolonged the survival time of rats bearing intracranial C6 glioma, when compared to paclitaxel conjugated nanoparticles and a commercial drug Taxol [274]. Ahmed et al., Double-receptor-targeting multifunctional iron oxide nanoparticles drug delivery system for the treatment and imaging of prostate cancer. Fuster MG, Montalbn MG, Moulefera I, Vllora G, Kaplan DL. Nanoparticles are classified into several main categories. 2019 Dec;33(6):1071-1093. doi: 10.1016/j.hoc.2019.08.002. Kirpotin et al., Antibody targeting of long-circulating lipidic nanoparticles does not increase tumor localization but does increase internalization in animal models. Int. Similarly, complete tumor eradication has been achieved employing cut-single walled carbon nanotubes coated with BSA-reduced Au nanoparticles, enhancing doxorubicin drug release when combined with phototherapy with an 808nm laser in a nude mouse model [202]. Linear type of FC131 (LFC131) ligand conjugated, doxorubicin encapsulated polyamide amine dendrimer was developed using polyamide amine dendrimer generation 4.0 (D4). Keywords: Daima, Contemporary developments in nanobiotechnology: applications, toxicity, sustainability and future perspective, in Nanobiotechnology: human health and the environment, ed. 25(17), 24892500 (2015), Y. Chen et al., Multifunctional envelope-type mesoporous silica nanoparticles for pH-responsive drug delivery and magnetic resonance imaging. From the above discussion, it can be concluded that nanomaterials for therapeutic applications need to be engineered carefully with respect to their size and shape, because both of them have noteworthy impact on the uptake process of cells, and can potentially induce cellular responses. Privacy The cytotoxicity assay demonstrated that resveratrol conjugated poly(lactic-co-glycolic acid) nanoparticles had two-fold lower IC50 and IC90 values in comparison to only resveratrol [253]. 9(2), 194201 (2013), P.M. Valencia et al., Effects of ligands with different water solubilities on self-assembly and properties of targeted nanoparticles. A comprehensive set of guidelines for regulatory approval is urgently needed to expedite the evaluation and approval of cancer nanotherapeutics. The ensuing section discusses major physicochemical properties of nanomaterials and their design considerations for therapeutic and diagnostic applications. Nat. 11, 31593166 (2016), P.-C. Liang et al., Doxorubicin-modified magnetic nanoparticles as a drug delivery system for magnetic resonance imaging-monitoring magnet-enhancing tumor chemotherapy. 2018;68:394. doi: 10.3322/caac.21492. Rep. 6, 28983 (2016), J. Nie, Y. Wang, W. Wang, In vitro and in vivo evaluation of stimuli-responsive vesicle from PEGylated hyperbranched PAMAM-doxorubicin conjugate for gastric cancer therapy. 5(1), 172182 (2013), D. Bobo et al., Nanoparticle-based medicines: a review of FDA-approved materials and clinical trials to date. Res. Please enable it to take advantage of the complete set of features! Sci. Biopharm. Sci. 2023 Mar 25;11(4):733. doi: 10.3390/vaccines11040733. These are responsive to pH, temperature, enzyme, light, the concentration of glutathione [283]. Despite the numerous advantages of the nano-based cancer therapeutics, clinical translation of these nanomedicines remains to be a challenging mission. PLoS ONE 12(8), e0181944e0181944 (2017), R.M. Med. It is anticipated that the nanomaterials will revolutionize the entire health care system based on the dramatic developments made in drug delivery sector over the past few decades. Folic Acid-Modified Ibrutinib-Loaded Silk Fibroin Nanoparticles for Cancer Cell Therapy with Over-Expressed Folate Receptor. Google Scholar, D. Xiao et al., A redox-responsive mesoporous silica nanoparticle capped with amphiphilic peptides by self-assembly for cancer targeting drug delivery. Rezaianzadeh A, Jalali M, Maghsoudi A, Mokhtari AM, Azgomi SH, Dehghani SL. Ovarian cancer (OC) is the seventh most common cancer in women worldwide. Amongst the widely used strategies, today in cancer research is nanotechnology. https://www.cancer.org/research/cancer-facts-statistics/all-cancer-facts Wu S, Zhu W, Thompson P, Hannun YA. Specifically, cationic magnetic nanoparticles are retained by the cells for extended period, inducing no cytotoxicity [116]. Liu et al., developed graphene oxide modified with chitosan followed by conjugation with hyaluronic acid and an anti-cancer drug SNX-2112. Due to the lack of understanding of toxicity and in vivo behaviour of nanoformulations, clinical trials are experiencing major setbacks. Hence nanotechnology has a deep impact on the environment. Before Similarly accumulating a high degree of hydrophobicity on the nanoparticles led to increased susceptibility towards macrophage uptake, without offering a significant advantage for rapid target cell internalization [57]. Chem. Additionally, mesoporous silica nanomaterials can release cargo in response to stimuli. Such thoughtful knowledge will be useful in the rational tailoring of nanomaterials, which can be used for personalized tumor medicine for even higher therapeutic benefits. Several studies have demonstrated enhanced antitumor activity with targeting moieties. Mater. Interfaces 9(4), 39853994 (2017), K. Yin Win, S.-S. Feng, Effects of particle size and surface coating on cellular uptake of polymeric nanoparticles for ral delivery of anticancer drugs. They have measured the cumulative release of loaded doxorubicin drug in different pH concentrations to confirm the functionality of the system [68]. Jeong, S. Jon, A drug-loaded aptamergold nanoparticle bioconjugate for combined CT imaging and therapy of prostate cancer. ACS Appl. Chem. 13, 24052426 (2018), B. Xiao et al., Co-delivery of camptothecin and curcumin by cationic polymeric nanoparticles for synergistic colon cancer combination chemotherapy. 2020 Dec 15;591:119986. doi: 10.1016/j.ijpharm.2020.119986. Nanoscale 9(43), 1706317073 (2017), X. Xu, F. Hu, Q. Shuai, Facile synthesis of highly biocompatible folic acid-functionalised SiO2 nanoparticles encapsulating rare-earth metal complexes, and their application in targeted drug delivery. The in vitro cytotoxicity studies revealed that doxorubicin formulations had increased antiproliferative effect and was time and dose-dependent as depicted in Fig. Normally, given the complexity of nanoparticles administration routes and undesirable interactions with non-specific molecules within the organisms, the difference in the nanoparticles affinity towards cancerous and normal cells would not be sufficient for high specificity and efficient delivery to the target site required for wide utility for biomedical applications. Since tumor blood flow is low compared to observed in other organs and bodily tissues, the increased affinity based on the ligands cannot compensate for the clearance processes [32]. Biol. What are the disadvantages of using nanotechnology in water and Res. 5 [103]. The structure of liposomes can be engineered to encapsulate the hydrophobic or hydrophilic drugs, or other small molecules, in the lipid bilayer or aqueous core, respectively [230]. J. Mol. 520(1), 126138 (2017), C.T. J. Pharm. 4. Small 6(20), 22612265 (2010), Y.B. IET Nanobiotechnol. Cho et al., Understanding the role of surface charges in cellular adsorption versus internalization by selectively removing gold nanoparticles on the cell surface with a I2/KI Etchant. Biomaterials 32(26), 62266233 (2011), L. Vroman, Effect of adsorbed proteins on the wettability of hydrophilic and hydrophobic solids. These particles can selectively target human osteosarcoma cells and are capable of pH-responsive antitumor drug delivery. B Biol. Scale bar: 200nm (b); in vitro cytotoxicity effect of different nanocomplexes on C6 cells evaluated by CCK8 assay at various TMZ concentrations. Rev. Du et al., Tailor-made dual pH-sensitive polymerdoxorubicin nanoparticles for efficient anticancer drug delivery. The designing of multifunctional delivery platforms using mesoporous silica nanomaterials with different characteristics is possible because of facile modification of their surface. Artif. 6 [188]. 171, 133138 (2017), A.A. Bhirde et al., Targeted killing of cancer cells in vivo and in vitro with EGF-directed carbon nanotube-based drug delivery. The critical aspect to this conjugation is to maintain the stability of the conjugated ligands during the adverse environment presented by the physiological environment, and various approaches have been undertaken to achieve it [32]. Sci. 58, 349364 (2017), Y. Peng et al., Codelivery of temozolomide and siRNA with polymeric nanocarrier for effective glioma treatment. 65, 393404 (2018), H.K. World J Hepatol. J. Liposome Res. Sci. Eur. Nanoparticles as a Delivery System of Antigens for the Development of an Effective Vaccine against. Several researchers have demonstrated that half-generation dendrimers exhibit lower toxicity than the full generation of polyamide amine [277,278,279]. Kam, Z. Liu, H. Dai, Functionalization of carbon nanotubes via cleavable disulfide bonds for efficient intracellular delivery of siRNA and potent gene silencing. -. Rep. 8(1), 2907 (2018), S. Patra et al., Green synthesis, characterization of gold and silver nanoparticles and their potential application for cancer therapeutics. Current trends and challenges in cancer management and therapy using designer nanomaterials, https://doi.org/10.1186/s40580-019-0193-2, http://creativecommons.org/licenses/by/4.0/.

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disadvantages of nanotechnology in cancer treatment

disadvantages of nanotechnology in cancer treatment