A review of DNA nanoparticles-encapsulated drug/gene/protein for advanced controlled drug release: Current status and future perspective over emerging therapy approaches

被引:11
作者
Kashani, Ghazal Kadkhodaie [1 ]
Naghib, Seyed Morteza [1 ]
Soleymani, Sina [1 ,2 ,3 ]
Mozafari, M. R. [2 ]
机构
[1] Iran Univ Sci & Technol IUST, Sch Adv Technol, Nanotechnol Dept, Tehran 1684613114, Iran
[2] Monash Univ LPO, Australasian Nanosci & Nanotechnol Initiat ANNI, Clayton, Vic 3168, Australia
[3] Iran Univ Sci & Technol IUST, Motamed Canc Inst, Breast Canc Res Ctr,ACECR, Interdisciplinary Technol Dept,Biomat & Tissue Eng, Tehran, Iran
关键词
DNA; Nanoparticles; Encapsulation; Drug delivery; Gene delivery; Controlled drug release; ORIGAMI NANOSTRUCTURES; DELIVERY SYSTEM; INTRACELLULAR DELIVERY; APTAMER; NANOTECHNOLOGY; THERAPEUTICS; DOXORUBICIN; MECHANISM; DESIGN; ARRAYS;
D O I
10.1016/j.ijbiomac.2024.131694
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last ten years, the field of nanomedicine has experienced significant progress in creating novel drug delivery systems (DDSs). An effective strategy involves employing DNA nanoparticles (NPs) as carriers to encapsulate drugs, genes, or proteins, facilitating regulated drug release. This abstract examines the utilization of DNA NPs and their potential applications in strategies for controlled drug release. Researchers have utilized the distinctive characteristics of DNA molecules, including their ability to self-assemble and their compatibility with living organisms, to create NPs specifically for the purpose of delivering drugs. The DNA NPs possess numerous benefits compared to conventional drug carriers, such as exceptional stability, adjustable dimensions and structure, and convenient customization. Researchers have successfully achieved a highly efficient encapsulation of different therapeutic agents by carefully designing their structure and composition. This advancement enables precise and targeted delivery of drugs. The incorporation of drugs, genes, or proteins into DNA NPs provides notable advantages in terms of augmenting therapeutic effectiveness while reducing adverse effects. DNA NPs serve as a protective barrier for the enclosed payloads, preventing their degradation and extending their duration in the body. The protective effect is especially vital for delicate biologics, such as proteins or gene-based therapies that could otherwise be vulnerable to enzymatic degradation or quick elimination. Moreover, the surface of DNA NPs can be altered to facilitate specific targeting towards particular tissues or cells, thereby augmenting the accuracy of delivery. A significant benefit of DNA NPs is their capacity to regulate the kinetics of drug release. Through the manipulation of the DNA NPs structure, scientists can regulate the rate at which the enclosed cargo is released, enabling a prolonged and regulated dispensation of medication. This control is crucial for medications with limited therapeutic ranges or those necessitating uninterrupted administration to attain optimal therapeutic results. In addition, DNA NPs have the ability to react to external factors, including alterations in temperature, pH, or light, which can initiate the release of the payload at precise locations or moments. This feature enhances the precision of drug release control. The potential uses of DNA NPs in the controlled release of medicines are extensive. The NPs have the ability to transport various therapeutic substances, for example, drugs, peptides, NAs (NAs), and proteins. They exhibit potential for the therapeutic management of diverse ailments, including cancer, genetic disorders, and infectious diseases. In addition, DNA NPs can be employed for targeted drug delivery, traversing biological barriers, and surpassing the constraints of conventional drug administration methods.
引用
收藏
页数:30
相关论文
共 284 条
[1]   DNA-Based Applications in Nanobiotechnology [J].
Abu-Salah, Khalid M. ;
Ansari, Anees A. ;
Alrokayan, Salman A. .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010,
[2]   Controlled Drug Delivery Systems: Current Status and Future Directions [J].
Adepu, Shivakalyani ;
Ramakrishna, Seeram .
MOLECULES, 2021, 26 (19)
[3]   Aptamer-functionalized Fe3O4@MOF nanocarrier for targeted drug delivery and fluorescence imaging of the triple-negative MDA-MB-231 breast cancer cells [J].
Alijani, Hamed ;
Noori, Abolhassan ;
Faridi, Nassim ;
Bathaie, S. Zahra ;
Mousavi, Mir F. .
JOURNAL OF SOLID STATE CHEMISTRY, 2020, 292
[4]   Next-generation engineered nanogold for multimodal cancer therapy and imaging: a clinical perspectives [J].
Alle, Madhusudhan ;
Sharma, Garima ;
Lee, Seung-Hwan ;
Kim, Jin-Chul .
JOURNAL OF NANOBIOTECHNOLOGY, 2022, 20 (01)
[5]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[6]   Self-assembly of a nanoscale DNA box with a controllable lid [J].
Andersen, Ebbe S. ;
Dong, Mingdong ;
Nielsen, Morten M. ;
Jahn, Kasper ;
Subramani, Ramesh ;
Mamdouh, Wael ;
Golas, Monika M. ;
Sander, Bjoern ;
Stark, Holger ;
Oliveira, Cristiano L. P. ;
Pedersen, Jan Skov ;
Birkedal, Victoria ;
Besenbacher, Flemming ;
Gothelf, Kurt V. ;
Kjems, Jorgen .
NATURE, 2009, 459 (7243) :73-U75
[7]  
[Anonymous], 1981, Ann. Intern. Med., V94, DOI [10.7326/0003-4819-94-6-8262, DOI 10.7326/0003-4819-94-6-8262]
[8]   Biodegradable nanoparticles as drug delivery devices [J].
Anwar, Maira ;
Muhammad, Faqir ;
Akhtar, Bushra .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2021, 64
[9]   Self-assembled pH-responsive DNA nanosponges for targeted co-delivery of doxorubicin and capsaicin for colorectal cancer therapy [J].
Asakiya, Charles ;
Zhang, Yangzi ;
Zhu, Liye ;
Ackah, Michael ;
Tavakoli, Samad ;
Zhu, Longjiao ;
Huang, Kunlun ;
Xu, Wentao .
BIOCHEMICAL ENGINEERING JOURNAL, 2023, 195
[10]   An aptamer-doxorubicin physical conjugate as a novel targeted drug-delivery platform [J].
Bagalkot, Vaishali ;
Farokhzad, Omid C. ;
Langer, Robert ;
Jon, Sangyong .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (48) :8149-8152