Ijraset Journal For Research in Applied Science and Engineering Technology
Authors: Priyanka Dhotre , Rohan Mane
DOI Link: https://doi.org/10.22214/ijraset.2026.77295
Certificate: View Certificate
Nanotechnology hold tremendous potential as an effective drug delivery system. In this review we discussed recent developments in nanotechnology for drug delivery. To overcome the problems of gene and drug delivery, nanotechnology has gained interest in recent years. Nanosystems with different compositions and biological properties have been extensively investigated for drug and gene delivery applications. To achieve efficient drug delivery it is important to understand the interactions of nanomaterials with the biological environment, targeting cell-surface receptors, drug release, multiple drug administration, stability of therapeutic agents and molecular mechanisms of cell signalling involved in pathobiology of the disease under consideration. Several anti-cancer drugs including paclitaxel, doxorubicin, 5-fluorouracil and dexamethasone have been successfully formulated using nanomaterials. Quantom dots, chitosan, Polylactic/glycolic acid (PLGA) and PLGA-based nanoparticles have also been used for in vitro RNAi delivery. Brain cancer is one of the most difficult malignancies to detect and treat mainly because of the difficulty in getting imaging and therapeutic agents past the blood-brain barrier and into the brain. Anti-cancer drugs such as loperamide and doxorubicin bound to nanomaterials have been shown to cross the intact blood-brain barrier and released at therapeutic concentrations in the brain. The use of nanomaterials including peptide-based nanotubes to target the vascular endothelial growth factor (VEGF) receptor and cell adhesion molecules like integrins, cadherins and selectins, is a new approach to control disease progression.
Nanotechnology has emerged as a powerful approach to improve drug delivery, diagnosis, and treatment of complex diseases. Nanoparticles, typically smaller than 100 nm, are made from biodegradable polymers, lipids, or metals and are taken up by cells far more efficiently than larger particles. Drugs can be encapsulated within nanoparticles or attached to their surfaces, allowing controlled, targeted delivery and improved therapeutic efficacy. Nanotechnology overcomes major limitations of conventional drug delivery systems, such as poor bioavailability, instability, low solubility, rapid degradation, systemic side effects, and plasma concentration fluctuations.
Nanoparticle-based drug delivery systems enhance oral bioavailability, protect drugs from degradation, enable sustained and targeted release, bypass first-pass metabolism, and reduce side effects. Their small size allows efficient tissue penetration and cellular uptake, making them particularly valuable for treating chronic diseases such as cancer, diabetes, cardiovascular diseases, asthma, and HIV. Advances in nanosystems have also enabled delivery of poorly water-soluble drugs and improved patient adherence while lowering healthcare costs.
Nanotechnology has been extensively applied in cancer therapy through targeted drug delivery, overcoming drug resistance, crossing biological barriers such as the blood–brain barrier, and inhibiting angiogenesis. Nanoparticles loaded with anticancer drugs like paclitaxel and doxorubicin have demonstrated improved efficacy and reduced toxicity, as seen in FDA-approved formulations such as Abraxane® and Doxil®. Targeting strategies using ligands, peptides, antibodies, and surface modifications such as PEGylation enhance tumor specificity and circulation time.
Nanoparticles also play a crucial role in gene therapy, particularly in siRNA delivery, by improving stability, cellular uptake, and tracking of gene silencing mechanisms. Fluorescent and quantum-dot-labeled nanoparticles enable monitoring of intracellular delivery and therapeutic effectiveness.
In inflammatory and infectious diseases, nanoparticles are used to target macrophages and inflammatory molecules, enabling effective intracellular delivery of antimicrobial and anti-inflammatory agents while minimizing systemic toxicity. Smart drug delivery systems (SDDS), also known as stimuli-responsive systems, release drugs in response to internal or external triggers such as pH, temperature, enzymes, or light, allowing “release-on-demand” and enhanced therapeutic precision.
Nanotechnology has also revolutionized medical imaging and diagnostics by improving contrast agents for imaging modalities such as MRI, CT, and optical imaging. Nanomaterials like gold nanoshells offer enhanced resolution, specificity, and reduced toxicity, enabling early disease detection and monitoring of treatment progress.
In cardiovascular disease management, nanoparticle-based systems improve drug targeting, reduce inflammation, enhance thrombolysis, and lower drug-related side effects. Liposomes, dendrimers, and polymeric nanoparticles have shown promise in treating atherosclerosis, thrombosis, and restenosis.
Despite these advances, potential risks associated with nanotechnology—particularly related to toxicity, environmental impact, and long-term health effects—remain a concern. While only certain highly reactive nanomaterials pose significant risks, further research is needed to fully understand and regulate their safety.
Overall, nanotechnology represents a transformative platform for drug delivery, diagnosis, and therapy, offering enhanced specificity, efficacy, and safety, while continuing research is essential to address remaining challenges and risks.
It appears that nano drug delivery systems hold great potential to overcome some of the barriers to efficient targeting of cells and molecules in inflammation and cancer. There also is an exciting possibility to overcome problems of drug resistance in target cells and to facilitating movement of drugs across barriers such as those in the brain. The challenge, however, remains the precise characterization of molecular targets and to ensure that these molecules are expressed only in the targeted organs to prevent effects on healthy tissues. Secondly, it is important to understand the fate of the drugs once delivered to the nucleus and to cause nanosystems increase efficiency of drug delivery, the doses may need recalibration. Nevertheless, the future remains exciting and wide open. There is no doubt that nanotechnologies have helped to improve the quality of life of patients by providing a platform for advances in biotechnological, medicinal and pharmaceutical industries. They have also facilitated healthcare procedures, from diagnosis to therapeutic interventions and follow-up monitoring. There is a constant push to create and develop novel nanomaterials to improve diagnosis and cures for diseases in a targeted, accurate, potent and long-lasting manner, with the ultimate aim of making medical practices more personalised, cheaper and safer.
[1] Pison U, Welte T, Giersing M, Groneberg DA. Nanomedicine for respiratory diseases. Eu J Pharmacology. 2006;533:341–350. doi: 10.1016/j.ejphar.2005.12.068. [DOI] [PubMed] [Google Scholar] [2] Brannon-Peppase L, Blanchette JQ. Nanoparticle and targeted systems for cancer therapy. Adv Drug Deliv Rev. 2004;56:1649–1659. doi: 10.1016/j.addr.2004.02.014. [DOI] [PubMed] [Google Scholar] [3] Stylios GK, Giannoudis PV, Wan T. Applications of nanotechnologies in medical practice. Injury. 2005;36:S6–S13. doi: 10.1016/j.injury.2005.10.011. [DOI] [PubMed] [Google Scholar] [4] Yokoyama M. Drug targeting with nano-sized carrier systems. J Artif Organs. 2005;8:77–84. doi: 10.1007/s10047-005-0285-0. [DOI] [PubMed] [Google Scholar] [5] Schatzlein AG. Delivering cancer stem cell therapies – a role for nanomedicines? Eur J Cancer. 2006;42:1309–1315. doi: 10.1016/j.ejca.2006.01.044. [DOI] [PubMed] [Google Scholar] [6] Groneberg DA, rabe KF, Fischer A. Novel concepts of neuropeptide-based therapy: Vasoactive intestinal polypeptide and its receptors. Eu J Pharmacology. 2006;533:182–194. doi: 10.1016/j.ejphar.2005.12.055. [DOI] [PubMed] [Google Scholar] [7] Grady WM. Epigenetic events in the colorectum and in colon cancer. Biochem Soc Trans. 2005;33:684–688. doi: 10.1042/BST0330684. [DOI] [PubMed] [Google Scholar] [8] Ould-Ouali L, Noppe M, Langlois X, Willems B, Te Riele P, Timmerman P, Brewster ME, Arien A, Preat V. Self-assembling PEG-p(CL-co-TMC) copolymers for oral delivery of poorly water-soluble drugs: a case study with risperidone. J Control Release. 2005;102:657–668. doi: 10.1016/j.jconrel.2004.10.022. [DOI] [PubMed] [Google Scholar] [9] Kipp JE. The role of solid nanoparticle technology in the parenteral delivery of poorly water-soluble drugs. Int J Pharm. 2004;284:109–122. doi: 10.1016/j.ijpharm.2004.07.019. [DOI] [PubMed] [Google Scholar] [10] Fonseca C, Simoes S, Gaspar R. Paclitaxel-loaded PLGA nanoparticles: preparation, physicochemical characterization and in vitro anti-tumoral activity. J Control Release. 2002;83:273–286. doi: 10.1016/S0168-3659(02)00212-2. [DOI] [PubMed] [Google Scholar] [11] Koziara JM, Whisman TR, Tseng MT, Mumper RJ. In-vivo efficacy of novel paclitaxel nanoparticles in paclitaxel-resistant human colorectal tumors. J Control Release. 2006;112:312–319. doi: 10.1016/j.jconrel.2006.03.001. [DOI] [PubMed] [Google Scholar] [12] Yoo HS, Lee KH, Oh JE, Park TG. In vitro and in vivo anti-tumor activities of nanoparticles based on doxorubicin-PLGA conjugates. J Control Release. 2000;68:419–31. doi: 10.1016/S0168-3659(00)00280-7. [DOI] [PubMed] [Google Scholar] [13] Bhadra D, Bhadra S, Jain S, Jain NK. A PEGylated dendritic nanoparticulate carrier of fluorouracil. Int J Pharm. 2003;257:111–124. doi: 10.1016/S0378-5173(03)00132-7. [DOI] [PubMed] [Google Scholar] [14] Panyam J, Labhasetwar V. Sustained cytoplasmic delivery of drugs with intracellular receptors using biodegradable nanoparticles. Mol Pharm. 2004;1:77–84. doi: 10.1021/mp034002c. [DOI] [PubMed] [Google Scholar] [15] Koziara JM, Lockman PR, Allen DD, Mumper RJ. Paclitaxel nanoparticles for the potential treatment of brain tumors. J Control Release. 2004;99:259–269. doi: 10.1016/j.jconrel.2004.07.006. [DOI] [PubMed] [Google Scholar] [16] Chen AA, Derfus AM, Khetani SR, Bhatia SN. Quantum dots to monitor RNAi delivery and improve gene silencing. Nucleic Acids Res. 2005;33:e190. doi: 10.1093/nar/gni188. [DOI] [PMC free article] [PubMed] [Google Scholar] [17] Shinde RR, Bachmann MH, Wang Q, Kasper R, Contag CH. PEG-PLA/PLGA Nanoparticles for In-Vivo RNAi Delivery. NSTI Nano tech., California; 2007. [Google Scholar] [18] Tan WB, Jiang S, Zhang Y. Quantum-dot based nanoparticles for targeted silencing of HER2/neu gene via RNA interference. Biomaterials. 2007;28:1565–1571. doi: 10.1016/j.biomaterials.2006.11.018. [DOI] [PubMed] [Google Scholar] [19] Howard KA, Rahbek UL, Liu X, Damgaard CK, Glud SZ, Andersen MØ, Hovgaard MB, Schmitz A, Nyengaard JR, Besenbacher F, Kjems J. RNA interference in vitro and in vivo using a novel chitosan/siRNA nanoparticle system. Mol Ther. 2006;14:476–484. doi: 10.1016/j.ymthe.2006.04.010. [DOI] [PubMed] [Google Scholar] [20] Kreuter J, Shamenkov D, Petrov V, Ramge P, Cychutek K, Koch-Brandt C, Alyautdin R. Apolipoprotein-mediated transport of nanoparticle-bound drugs across the blood-brain barrier. J Drug Target. 2002;10:317–325. doi: 10.1080/10611860290031877. [DOI] [PubMed] [Google Scholar] [21] Costantino L, Gandolfi F, Tosi G, Rivasi F, Vandelli MA, Forni F. Peptide-derivatized biodegradable nanoparticles able to cross the blood-brain barrier. J Control Release. 2005;108:84–96. doi: 10.1016/j.jconrel.2005.07.013. [DOI] [PubMed] [Google Scholar] [22] Sumner JP, Kopelman R. Alexa Fluor 488 as an iron sensing molecule and its application in PEBBLE nanosensors. Analyst. 2005;130:528–533. doi: 10.1039/b414189j. [DOI] [PubMed] [Google Scholar] [23] Michaelis K, Hoffmann MM, Dreis S, Herbert E, Alyautdin RN, Michaelis M, Kreuter J, Langer K. Covalent linkage of apolipoprotein e to albumin nanoparticles strongly enhances drug transport into the brain. J Pharmacol Exp Ther. 2006;317:1246–1253. doi: 10.1124/jpet.105.097139. [DOI] [PubMed] [Google Scholar] [24] Steiniger SC, Kreuter J, Khalansky AS, Skidan IN, Bobruskin AI, Smirnova ZS, Severin SE, Uhl R, Kock M, Geiger KD, Gelperina SE. Chemotherapy of glioblastoma in rats using doxorubicin-loaded nanoparticles. Int J Cancer. 2004;109:759–767. doi: 10.1002/ijc.20048. [DOI] [PubMed] [Google Scholar] [25] Zhang Y, Sun C, Kohler N, Zhang M. Self-Assembled Coatings on Individual Monodisperse Magnetite Nanoparticles for Efficient Intracellular Uptake. Biomedical Microdevices. 2004;6:33–40. doi: 10.1023/B:BMMD.0000013363.77466.63. [DOI] [PubMed] [Google Scholar] [26] Li L, Wartchow CA, Danthi SN, Shen Z, Dechene N, Pease J, Choi HS, Doede T, Chu P, Ning S, Lee DY, Bednarski MD, Knox SJ. A Novel Antiangiogenesis Therapy Using an Integrin Antagonist or Anti-Flk-1 Antibody Coated 90Y-labeled Nanoparticles. Int J Radiat Oncol Biol Phy. 2004;58:1215–1227. doi: 10.1016/j.ijrobp.2003.10.057. [DOI] [PubMed] [Google Scholar] [27] Park JH, Kwon S, Nam JO, Park RW, Chung H, Seo SB, Kim IS, Kwon IC, Jeong SY. Self-assembled nanoparticles based on glycol chitosan bearing 5beta-cholanic acid for RGD peptide delivery. J Control Release. 2004;95:579–588. doi: 10.1016/j.jconrel.2003.12.020. [DOI] [PubMed] [Google Scholar] [28] Fenniri H, Deng BL, Ribbe AE, Hallenga K, Jacob J, Thiyagarajan P. Entropically driven self-assembly of multichannel rosette nanotubes. Proc Nat Acad Sci. 2002;99:6487–6492. doi: 10.1073/pnas.032527099. [DOI] [PMC free article] [PubMed] [Google Scholar] [29] Fenniri H, Mathivanan P, Vidale KL, Sherman DM, Hallenga K, Wood KV, Stowell JG. Helical rosette nanotubes: design, self-assembly, and characterization. J Am Chem Soc. 2001;123:3854–3855. doi: 10.1021/ja005886l. [DOI] [PubMed] [Google Scholar]
Copyright © 2026 Priyanka Dhotre , Rohan Mane . This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Paper Id : IJRASET77295
Publish Date : 2026-02-04
ISSN : 2321-9653
Publisher Name : IJRASET
DOI Link : Click Here
Submit Paper Online
