Drug Nanocrystals in Oral Absorption: Factors That Influence Pharmacokinetics DOI Creative Commons
Luiza de O. Macedo, Jéssica Fagionato Masiero, Nádia Araci Bou‐Chacra

et al.

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(9), P. 1141 - 1141

Published: Aug. 29, 2024

Despite the safety and convenience of oral administration, poorly water-soluble drugs compromise absorption bioavailability. These can exhibit low dissolution rates, variability between fed fasted states, difficulty permeating mucus layer, P-glycoprotein efflux. Drug nanocrystals offer a promising strategy to address these challenges. This review focuses on opportunities develop orally administered based pharmacokinetic outcomes. The impacts drug particle size, morphology, rate, crystalline state bioavailability are discussed. potential improved rate eliminate food effects during is also addressed. explores whether permeation or drives nanocrystal absorption. Additionally, it addresses functional roles stabilizers. may result in prolonged concentrations bloodstream some cases. Therefore, represent overcome challenges drugs, thus encouraging further investigation into unclear mechanisms administration.

Language: Английский

Improved Cognitive Impairment Through PLGA Nanocrystal-Based Drug Delivery of Curcumin and Piperine in Alzheimer's Disease Model DOI Creative Commons
Zhi Xin Phuna, Shantini Vijayabalan, Bibhu Prasad Panda

et al.

Research Square (Research Square), Journal Year: 2025, Volume and Issue: unknown

Published: March 27, 2025

Abstract Alzheimer’s disease (AD) is a multifactorial neurodegenerative that causes dementia, impaired cognitive function, and disorientation. Studies have revealed curcumin piperine were found to be neuroprotective for patients with dementia. Nevertheless, both compounds are known their poor solubility. To address issues related bioavailability, nanocrystals of in combination fabricated characterized by physicochemical, surface morphology, drug excipient compatibilities, bioavailability studies. The nanocrystal the highest was selected pharmacokinetics pharmacodynamics Optimized PLGA co-loaded (FNC) successfully developed using emulsion diffusion-high pressure homogenization-solvent evaporation (EHS) technique Poloxamer 188 as stabilizer. Among nine formulations, optimized FNC1 had particle size 116.6 ± 2.13 nm zeta potential at -27.9 1.51 mV. Saturation solubility in vitro release studies demonstrated enhanced compared pure compounds. Oral administration streptozotocin (STZ)-induced AD rat model presented significant improvement spatial memory from Morris Water Maze Passive Avoidance test. Further histology staining cortex hippocampus regions significantly reduced number pyramidal cells extensive nuclear pyknosis degeneration previously seen untreated STZ-induced rats. It concluded this study improved which then impairment

Language: Английский

Citations

0

Nanocrystals in Dermal Drug Delivery: A Breakthrough for Enhanced Skin Penetration and Targeted Skin Disorder Treatments DOI Creative Commons
Ahmed Alnaim

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(12), P. 1561 - 1561

Published: Dec. 6, 2024

One of the major challenges in dermal drug delivery is adequate penetration active compound into skin without causing any irritation and inflammation. Nanocrystals (NCs) are nanoscale particles, their sizes below 1000 nm. NCs made up particles only, which used to improve aqueous solubility bioavailability poorly water-soluble drugs. typically prepared either by bottom-up or top-down techniques. The advantages using NC-based formulations enhancing include increased loading capacity, easier deeper tissue, passive diffusion. with capacity enhanced can be effectively treat a wide range disorders, including melanoma, inflammation, psoriasis, acne vulgaris, bacterial infections, fungal eczema, aging, herpes simplex virus manifestations tick bites, frostbite-related hyperpigmentation, diabetic foot ulcer. In this review, across barrier, mechanism action NCs, delivery, NC preparation methods, applications treatment various disorders have been discussed.

Language: Английский

Citations

3

Drug Nanocrystals in Oral Absorption: Factors That Influence Pharmacokinetics DOI Creative Commons
Luiza de O. Macedo, Jéssica Fagionato Masiero, Nádia Araci Bou‐Chacra

et al.

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(9), P. 1141 - 1141

Published: Aug. 29, 2024

Despite the safety and convenience of oral administration, poorly water-soluble drugs compromise absorption bioavailability. These can exhibit low dissolution rates, variability between fed fasted states, difficulty permeating mucus layer, P-glycoprotein efflux. Drug nanocrystals offer a promising strategy to address these challenges. This review focuses on opportunities develop orally administered based pharmacokinetic outcomes. The impacts drug particle size, morphology, rate, crystalline state bioavailability are discussed. potential improved rate eliminate food effects during is also addressed. explores whether permeation or drives nanocrystal absorption. Additionally, it addresses functional roles stabilizers. may result in prolonged concentrations bloodstream some cases. Therefore, represent overcome challenges drugs, thus encouraging further investigation into unclear mechanisms administration.

Language: Английский

Citations

0