Evidence map›Paper›PMID 39099216›Full record

ArticleRecent patents on nanotechnology2025

Formulation Optimization and Characterization of Solid Lipid Nanoparticles of Apixaban.

Laukik Mulay, Namita Hegde, Abhishek Kanugo

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Article in Recent patents on nanotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3 citing papers in PubMed.

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5 · Who and what money

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3 authors.

Laukik MulayDepartment of Pharmaceutics, SVKM NMIMS School of Pharmacy and Technology Management, Shirpur, 425405, Dhule, India.
Namita HegdeDepartment of Pharmaceutics, SVKM NMIMS Shobhaben Pratapbhai Patel School of Pharmacy and Technology Management, Mumbai, 400056, India.
Abhishek KanugoDepartment of Pharmaceutics, SVKM NMIMS School of Pharmacy and Technology Management, Shirpur, 425405, Dhule, India.ORCID 0000-0002-5205-5906

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnpredictable situations such as clotting of blood, deep vein thrombosis, and pulmonary embolism arise in the body, which is the leading cause of mortality. Such conditions generally arise after surgery as well as after treatment with oral anticoagulant agents. Apixaban is a novel oral anticoagulant widely recommended for the prevention and treatment of strokes and blood clots suffering from nonvalvular atrial fibrillation by suppressing factor Xa. Apixaban has a log P of 2.71 with poor solubility and reported maximum bioavailability of approximately 50%.

objectiveHence, the current research mainly focused on the improvement of solubility, bioavailability, and therapeutic efficacy of Apixaban via solid lipid nanoparticles (SLN).

methodsThe SLN was developed using the hot-homogenization method using a high-pressure homogenizer. The drug-lipid compatibility study was assessed by the FTIR, and the thermal analysis was performed using differential scanning calorimetry (DSC). During the scrutiny of lipids, the highest solubility of Apixaban was estimated in the glyceryl monostearate, hence selected for the formulation. Moreover, the colloidal solution was stabilized by the polyethylene glycol 200. The Design of Expert software (Version 13, Stat-Ease) was implemented for the optimization analysis by considering the 3-independent factors and 2-dependent parameters. The Patents on the SLN are Indian 202321053691, U.S. Patent, 10,973,798B2, U.S. Patent, U.S. Patent 2021/0069121A1, U.S. Patent 2022/0151945A1.

resultsBox-Behnken design was applied along with ANOVA, which showed a p-value less than 0.05 for the dependent parameters such as particle size and entrapment efficiency (p-value: 0.0476 and 0.0379). The optimized batch F10 showed a particle size of 167.1 nm, -19.5 mV zeta potential, and an entrapment efficiency of 87.32%. The optimized batch F10 was lyophilized and analyzed by Scanning electron microscopy (SEM), which showed a particle size of 130 nm. The solid powder was filled into the capsule for oral delivery.

conclusionThe marked improvement in solubility and bioavailability was achieved with F10- loaded Apixaban via Solid lipid nanoparticles. Moreover, the sustained released profile also minimizes the unseen complications that occur due to the clotting of blood.

Indexed as

LipidsNanoparticlesPyrazolesPyridonesBiological AvailabilityDrug CompoundingHumansParticle SizeSolubilityapixabanLipidsPyrazolesPyridonesApixabanBox-behnken designdeep vein thrombosisDSCFTIRhot-homogenization methodSEM.solid lipid nanoparticles

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.