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Development of solid lipid nanoparticles-loaded drugs in parasitic diseases.

作者信息

Nemati Sara, Mottaghi Mahsa, Karami Parisa, Mirjalali Hamed

机构信息

Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Biology, Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

出版信息

Discov Nano. 2024 Jan 4;19(1):7. doi: 10.1186/s11671-023-03955-w.


DOI:10.1186/s11671-023-03955-w
PMID:38175309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10767167/
Abstract

Parasites cause illnesses with broad spectrum of symptoms from mild to severe, and are responsible for a significant number of outbreaks in the world. Current anti-parasitic drugs are toxic and have significant side effects. Nano-carriers are believed to obviate the limitations of conventional drugs via decreasing side effects and increasing target delivery and drug permeability with a controlled prolonged release of a drug. Solid lipid nanoparticles (SLNs) are lipid nanoparticles (LNPs), which have frequently been practiced. Suitable release rate, stability, and target delivery make SLNs a good alternative for colloidal carriers. SLNs are supposed to have great potential to deliver natural products with anti-parasitic properties. Nanoparticles have employed to improve stability and capacity loading of SLNs, during recent years. This review describes development of SLNs, the methods of preparation, characterization, and loaded drugs into SLNs in parasitic diseases. In addition, we summarize recent development in anti-parasitic SLNs-loaded drugs.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/10767167/2ed58f2d47d6/11671_2023_3955_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/10767167/c46393efedce/11671_2023_3955_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/10767167/2ed58f2d47d6/11671_2023_3955_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/10767167/c46393efedce/11671_2023_3955_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c32/10767167/2ed58f2d47d6/11671_2023_3955_Fig2_HTML.jpg

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[1]
Development of solid lipid nanoparticles-loaded drugs in parasitic diseases.

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引用本文的文献

[1]
Nanoparticle Strategies for Treating CNS Disorders: A Comprehensive Review of Drug Delivery and Theranostic Applications.

Int J Mol Sci. 2024-12-11

[2]
Effects of nanocapsules containing lumefantrine and artemether in an experimental model of cerebral malaria.

Discov Nano. 2024-11-14

[3]
A Comparative Review of Tocosomes, Liposomes, and Nanoliposomes as Potent and Novel Nanonutraceutical Delivery Systems for Health and Biomedical Applications.

Biomedicines. 2024-9-3

[4]
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Food Sci Nutr. 2024-2-20

本文引用的文献

[1]
Artemisinin-Resistant and HRP-Negative Malaria Parasites in Africa.

N Engl J Med. 2023-9-28

[2]
Plasmodium falciparum resistant to artemisinin and diagnostics have emerged in Ethiopia.

Nat Microbiol. 2023-10

[3]
Prevalence of intestinal parasitic infections in patients with diabetes: a systematic review and meta-analysis.

Int Health. 2024-1-2

[4]
Toward waterborne protozoa detection using sensing technologies.

Front Microbiol. 2023-2-24

[5]
Effects of helminths and anthelmintic treatment on cardiometabolic diseases and risk factors: A systematic review.

PLoS Negl Trop Dis. 2023-2

[6]
Malaria - Epidemiology, Treatment, and Prevention.

N Engl J Med. 2023-2-2

[7]
Opportunity in nanomedicine to counter the challenges of current drug delivery approaches used for the treatment of malaria: a review.

J Drug Target. 2023-4

[8]
Safety of Praziquantel and Albendazole Coadministration for the Control and Elimination of Schistosomiasis and Soil-Transmitted Helminths Among Children in Rwanda: An Active Surveillance Study.

Drug Saf. 2022-8

[9]
Mebendazole, an anti-helminth drug, suppresses inflammation, oxidative stress and injury in a mouse model of ulcerative colitis.

Sci Rep. 2022-6-17

[10]
Solid Lipid Nanoparticles for Efficient Oral Delivery of Tyrosine Kinase Inhibitors: A Nano Targeted Cancer Drug Delivery.

Adv Pharm Bull. 2022-3

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