To see or not to see: In vivo nanocarrier detection methods in the brain and their challenges DOI Creative Commons
Antonia Wehn,

Eva Krestel,

Biyan Nathanael Harapan

et al.

Journal of Controlled Release, Journal Year: 2024, Volume and Issue: 371, P. 216 - 236

Published: May 31, 2024

Nanoparticles have a great potential to significantly improve the delivery of therapeutics brain and may also be equipped with properties investigate function. The brain, being highly complex organ shielded by selective barriers, requires its own specialized detection system. However, significant hurdle achieve these goals is still identification individual nanoparticles within sufficient cellular, subcellular, temporal resolution. This review aims provide comprehensive summary current knowledge on systems for tracking across blood-brain barrier brain. We discuss commonly employed in vivo ex nanoparticle quantification methods, as well various imaging modalities able detect Advantages weaknesses biological factors that must considered when interpreting results obtained through nanotechnologies are summarized. Finally, we critically evaluate prevailing limitations existing technologies explore solutions.

Language: Английский

Progress in nasal drug delivery systems DOI
Flavia Laffleur,

Bettina Bauer

International Journal of Pharmaceutics, Journal Year: 2021, Volume and Issue: 607, P. 120994 - 120994

Published: Aug. 12, 2021

Language: Английский

Citations

127

Development and Optimization of Naringenin-Loaded Chitosan-Coated Nanoemulsion for Topical Therapy in Wound Healing DOI Creative Commons
Sabah H. Akrawi, Bapi Gorain, Anroop B. Nair

et al.

Pharmaceutics, Journal Year: 2020, Volume and Issue: 12(9), P. 893 - 893

Published: Sept. 20, 2020

The potential role of naringenin (NAR), a natural flavonoid, in the treatment chronic wound has prompted present research to deliver drug nanoemulsion (NE) form, where synergistic chitosan was achieved through development chitosan-coated NAR NE (CNNE). consisted Capryol 90, Tween 20 and Transcutol P, which fabricated by low-energy emulsification method encapsulate within oil core. optimization formulated NEs performed using Box-Behnken statistical design obtain crucial variable parameters that influence globule size, size distribution surface charge. Finally, optimized formulation coated with different concentrations subsequently characterized vitro. CNNE found be increased when drug-loaded chitosan. Controlled release characteristics depicted 67-81% from CNNE, compared 89% formulation. Cytotoxicity study vitro fibroblast cell line (NIH-3T3), no inhibition proliferation cells observed CNNE. healing evaluated an abrasion-created model experimental animals were treated histologically at 0 14 days. Significant improvement construction abrasion whereas stimulation skin regeneration histological examination. Therefore, it could summarized coating developed is platform accelerate wounds.

Language: Английский

Citations

97

Experimental design, formulation and in vivo evaluation of a novel topical in situ gel system to treat ocular infections DOI Creative Commons
Anroop B. Nair, Jigar Shah, Shery Jacob

et al.

PLoS ONE, Journal Year: 2021, Volume and Issue: 16(3), P. e0248857 - e0248857

Published: March 19, 2021

In situ gels have been extensively explored as ocular drug delivery system to enhance bioavailability and efficacy. The objective of present study was design, formulate evaluate ion-activated in gel the penetration therapeutic performance moxifloxacin ophthalmic delivery. A simplex lattice design utilized examine effect various factors on experimental outcomes system. influence polymers (independent variables) such gellan gum (X 1 ), sodium alginate 2 HPMC 3 ) strength, adhesive force, viscosity release after 10 h (Q were assessed. Selected formulation (MH7) studied for ex vivo permeation, irritation pharmacokinetics rabbits. Data revealed that increase concentration led higher force viscosity, however, decreases release. MH7 exhibited all physicochemical properties within acceptable limits stable 6 months. Release profile from comparable check point batches followed Korsmeyer-Peppas matrix diffusion-controlled mechanism. Ocular signifies selected is safe non-irritant administration. data indicates significant improvement ( p < 0.0001) MH7, evidenced by C max (727 ± 56 ng/ml) greater AUC (2881 108 ng h/ml), when compared with commercial eye drops (C ; 503 85 ng/ml AUC; 978 86 h/ml). conclusion, developed could offers a more effective extended therapy infections conventional drops.

Language: Английский

Citations

62

Nose-to-Brain Targeting via Nanoemulsion: Significance and Evidence DOI Creative Commons
Shashi Kiran Misra, Kamla Pathak

Colloids and Interfaces, Journal Year: 2023, Volume and Issue: 7(1), P. 23 - 23

Published: March 17, 2023

Background: Non-invasive and patient-friendly nose-to-brain pathway is the best-suited route for brain delivery of therapeutics as it bypasses blood–brain barrier. The intranasal (olfactory trigeminal nerves) allows entry various bioactive agents, delivers a wide array hydrophilic hydrophobic drugs, circumvents hepatic first-pass effect, thus targeting neurological diseases in both humans animals. olfactory nerves make bridge between highly vascularised nasal cavity tissues permeation distribution, presenting direct into brain. Materials: This review portrays insight recent research reports (spanning last five years) on nanoemulsions developed actives management myriad disorders, namely, Parkinson’s disease, Alzheimer’s, epilepsy, depression, schizophrenia, cerebral ischemia tumours. information data are collected compiled from more than one hundred Scopus- PubMed-indexed articles. Conclusions: pathways facilitate better biodistribution bypass BBB issues and, thus, pose possible alternative hydrophobic, poor absorption enzyme degradative therapeutics. Exploring these virtues, have proven to be active, non-invasiveand safe brain-targeting cargos alleviation other neurodegenerative disorders.

Language: Английский

Citations

24

Nanotechnologies for intranasal drug delivery: an update of literature DOI
Rosamaria Lombardo, Teresa Musumeci, Claudia Carbone

et al.

Pharmaceutical Development and Technology, Journal Year: 2021, Volume and Issue: 26(8), P. 824 - 845

Published: July 5, 2021

Scientific research has focused its attention on finding an alternative route to systemic oral and parenteral administration, overcome their usual drawbacks, such as hepatic first-pass which decreases drug bioavailability after off-target effects, low patient compliance speed of onset the pharmacological action in first-aid cases. Innovative delivery systems (DDS), mainly based polymer lipid biocompatible materials, have given a great prompt this direction last years. The intranasal (IN) administration is valid non-invasive alternative. It highly suitable for self-administration, quickly reaches bloodstream, largely avoiding first pass effect, can also reach directly brain bypassing BBB. Association IN with DDS thus become winning strategy controlled drugs, especially when very quick effect desired or needed. This review aims at analyzing scientific literature regarding IN-DDS different ways (systemic, topical, pulmonary, nose-to-brain). In particular, was devoted polymer- lipid-based micro- nanocarriers, being topic most published articles decade, but whole plethora colloidal investigated recent years presented.

Language: Английский

Citations

52

Critical Review of Lipid-Based Nanoparticles as Carriers of Neuroprotective Drugs and Extracts DOI Creative Commons
Filipe Fernandes, Mónica Dias-Teixeira, Cristina Delerue‐Matos

et al.

Nanomaterials, Journal Year: 2021, Volume and Issue: 11(3), P. 563 - 563

Published: Feb. 24, 2021

The biggest obstacle to the treatment of diseases that affect central nervous system (CNS) is passage drugs across blood-brain barrier (BBB), a physical regulates entry substances into brain and ensures homeostasis CNS. This review summarizes current research on lipid-based nanoparticles for nanoencapsulation neuroprotective compounds. A survey studies nanoemulsions (NEs), nanoliposomes/nanophytosomes solid lipid (SLNs)/nanostructured carriers (NLCs) was carried out discussed herein, with particular emphasis upon their unique characteristics, most important parameters influencing formulation each one, examples compounds/extracts nanoencapsulated using these nanoparticles. Gastrointestinal absorption also discussed, as it may pose some obstacles free compounds bloodstream, consequently hampering drug concentration in brain. transport mechanisms through which or cross BBB parenchyma, potential increase bioavailability, are discussed. Additionally, factors contributing disruption neurodegeneration described. Finally, advantages of, to, conventional unconventional routes administration deliver taking account avoidance first-pass metabolism, onset action, ability bypass

Language: Английский

Citations

48

Formulation and characterisation of deferoxamine nanofiber as potential wound dressing for the treatment of diabetic foot ulcer DOI

Tracey Anastacia Jeckson,

Yun Ping Neo, Sreenivas Patro Sisinthy

et al.

Journal of Drug Delivery Science and Technology, Journal Year: 2021, Volume and Issue: 66, P. 102751 - 102751

Published: Aug. 21, 2021

Language: Английский

Citations

46

Nose-to-brain delivery of amisulpride-loaded lipid-based poloxamer-gellan gum nanoemulgel: In vitro and in vivo pharmacological studies DOI
Dnyandev Gadhave,

Shrikant Tupe,

Amol Tagalpallewar

et al.

International Journal of Pharmaceutics, Journal Year: 2021, Volume and Issue: 607, P. 121050 - 121050

Published: Aug. 25, 2021

Language: Английский

Citations

42

Drug Nanocrystals: Focus on Brain Delivery from Therapeutic to Diagnostic Applications DOI Creative Commons
Elide Zingale, Angela Bonaccorso, Claudia Carbone

et al.

Pharmaceutics, Journal Year: 2022, Volume and Issue: 14(4), P. 691 - 691

Published: March 23, 2022

The development of new drugs is often hindered by low solubility in water, a problem common to nearly 90% natural and/or synthetic molecules the discovery pipeline. Nanocrystalline drug technology involves reduction bulk particle size down nanosize range, thus modifying its physico-chemical properties with beneficial effects on bioavailability. Nanocrystals (NCs) are carrier-free particles surrounded stabilizer and suspended an aqueous medium. Due high loading, NCs maintain potent therapeutic concentration produce desirable pharmacological action, particularly useful treatment central nervous system (CNS) diseases. In addition purpose, NC can be applied for diagnostic scope. This review aims provide overview application different administration routes, especially focusing brain targeting, particular attention fields. applications analyzed most CNS pathologies (i.e., Parkinson's disease, psychosis, Alzheimer's etc.). Recently, growing interest has emerged from use colloidal fluorescent diagnostics. Therefore, imaging vessels tumor cells also discussed. Finally, clinical effectiveness leading increasing number FDA-approved products, among which approved neurological disorders have increased.

Language: Английский

Citations

31

Nanosystems for Brain Targeting of Antipsychotic Drugs: An Update on the Most Promising Nanocarriers for Increased Bioavailability and Therapeutic Efficacy DOI Creative Commons

Maria Daniela Ferreira,

Joana Duarte, Francisco Veiga

et al.

Pharmaceutics, Journal Year: 2023, Volume and Issue: 15(2), P. 678 - 678

Published: Feb. 17, 2023

Orally administered antipsychotic drugs are the first-line treatment for psychotic disorders, such as schizophrenia and bipolar disorder. Nevertheless, adverse drug reactions jeopardize clinical outcomes, resulting in patient non-compliance. The design formulation strategies enhancing brain delivery has been a major challenge, mainly due to restrictive properties of blood-brain barrier. However, recent pharmacokinetic pharmacodynamic vivo assays confirmed advantage intranasal route when compared oral intravenous administration, it allows direct nose-to-brain transport via neuronal pathways, reducing systemic side effects maximizing therapeutic outcomes. In addition, incorporation into nanosystems polymeric nanoparticles, mixed micelles, solid lipid nanostructured carriers, nanoemulsions, nanoemulgels, nanosuspensions, niosomes spanlastics, proven be quite promising. developed nanosystems, having small homogeneous particle size (ideal delivery), high encapsulation efficiency good stability, resulted improved bioavailability therapeutic-like animal models. Hence, although is essential continue research this field, schizophrenia, disorder other related disorders promising, opening path future therapies with higher efficacy.

Language: Английский

Citations

15