RETRACTED ARTICLE: Evaluation of the anticancer potential of CD44 targeted vincristine nanoformulation in prostate cancer xenograft model: a multi-dynamic approach for advanced pharmacokinetic evaluation DOI Creative Commons
Faiza Naseer, Kousain Kousar, Maisa Siddiq Abduh

et al.

Cancer Nanotechnology, Journal Year: 2023, Volume and Issue: 14(1)

Published: June 20, 2023

Abstract The in vivo anticancer potential of vincristine (VC) loaded, thiolated chitosan-based nanoformulation (NFs) with an outer hyaluronic acid (VC-loaded TCs-HA) coating was studied prostate cancer (PC) xenograft the immunosuppressed rat model induced by PC3 cell lines. Our previous study has already reported vitro efficacy said NFs. ADMET Predictor (TM) Cloud version 10.4.0.5, 64-bit, used to simulate VC's physicochemical and pharmacokinetic parameters. percentage encapsulation efficiency VC direct indirect methods 81.5 90%, respectively. Plasma samples from healthy rats showed improved bioavailability profiles NFs compared injection via HPLC. haemolytic analysis two times lesser toxicity red blood cells. Xenograft maximum tumour volume up 235 ± 0.02 mm 3 increased body weight, it reduced 56 0.01 107.3 0.03 during whole treatment pure VC. histopathology group less malignancy angiogenesis significantly metastasis liver kidney. ELISA high expression apoptotic biomarkers, including Bax, cleaved Caspase 3, PARP, while BCL2, COX-II, NFκB, TNF-α reduced. Immunohistochemical also revealed that post-NF administration, cytoplasmic expressions COX-II were reduced, as nuclear NFκB. Thus, prepared chemotherapeutic a comparatively potent oncolytic agent, safe off-target toxicity, had profile.

Language: Английский

Chitosan: An overview of biological activities, derivatives, properties, and current advancements in biomedical applications DOI
Great Iruoghene Edo, Emad͏͏͏͏͏͏͏͏͏͏͏͏͏͏͏͏͏͏͏ Yousif, Mohammed H. Al‐Mashhadani

et al.

Carbohydrate Research, Journal Year: 2024, Volume and Issue: 542, P. 109199 - 109199

Published: June 27, 2024

Language: Английский

Citations

39

Chitosan in Oral Drug Delivery Formulations: A Review DOI Creative Commons
Tanikan Sangnim, Divya Dheer,

Nitin Jangra

et al.

Pharmaceutics, Journal Year: 2023, Volume and Issue: 15(9), P. 2361 - 2361

Published: Sept. 21, 2023

Nanoformulations have become increasingly useful as drug delivery technologies in recent decades. As therapeutics, oral administration is the most common method, although it not always effective route because of challenges with swallowing, gastrointestinal discomfort, low solubility, and poor absorption. One significant barriers that medications must overcome to exert a therapeutic effect impact first hepatic transit. Studies shown controlled-release systems using nanoparticles composed biodegradable natural polymers significantly improve administration, which why these materials attracted attention. Chitosan possesses wide variety properties functions pharmaceutical well healthcare industries. Drug encapsulation transport within body are two its important features. Moreover, chitosan can enhance efficacy by facilitating interaction target cells. Based on physicochemical properties, potentially be synthesized into nanoparticles, this review summarizes advances applications orally delivered nanoparticle interventions.

Language: Английский

Citations

25

Enhancing therapeutic efficacy: sustained delivery of 5-fluorouracil (5-FU) via thiolated chitosan nanoparticles targeting CD44 in triple-negative breast cancer DOI Creative Commons
Sadia Anjum, Faiza Naseer, Tahir Ahmad

et al.

Scientific Reports, Journal Year: 2024, Volume and Issue: 14(1)

Published: May 19, 2024

Our current study reports the successful synthesis of thiolated chitosan-based nanoparticles for targeted drug delivery 5-Fluorouracil. This process was achieved through ionic gelation technique, aiming to improve efficacy chemotherapeutic moiety by modifying surface (NPs) with a ligand. We coated these NPs hyaluronic acid (HA) actively target CD44 receptor, which is frequently overexpressed in various solid malignancies, including breast cancer. XRD, FTIR, SEM, and TEM were used physicochemical analysis NPs. These 5-Fluorouracil (5-FU) loaded evaluated on MDA-MB-231 (a triple-negative cell line) MCF-10A (normal epithelial cells) determine their vitro efficacy. The developed 5-FU-loaded exhibited particle size within favorable range (< 300 nm). positive zeta potential facilitated uptake negatively charged cancer cells. Moreover, they demonstrated robust stability high encapsulation efficiency. significant cytotoxicity compared crude (p < 0.05) displayed promising release pattern consistent basic diffusion model. traits pharmacokinetic profile, efficacy, ability precisely nanoparticles, offering potentially anticancer treatment However, additional vivo assessments formulations are obligatory confirm findings.

Language: Английский

Citations

14

Ultra-sensitive pH responsive hydrogels with injectable and self-healing performance for controlled drug delivery DOI Creative Commons
Yang Yu, Yili Zhao,

Yujiao Zou

et al.

International Journal of Pharmaceutics X, Journal Year: 2025, Volume and Issue: unknown, P. 100334 - 100334

Published: April 1, 2025

Language: Английский

Citations

1

Chitosan Nanoparticles for Targeted Cancer Therapy: A Review of Stimuli-Responsive, Passive, and Active Targeting Strategies DOI Creative Commons

Jafar R.M.H. Al-Shadidi,

Shahad Al-Shammari,

Danah Al-Mutairi

et al.

International Journal of Nanomedicine, Journal Year: 2024, Volume and Issue: Volume 19, P. 8373 - 8400

Published: Aug. 1, 2024

Despite all major advancements in drug discovery and development the pharmaceutical industry, cancer is still one of most arduous challenges for scientific community. The implications nanotechnology have certainly resolved issues related to conventional anticancer modalities; however, undesired recognition nanoparticles (NPs) by mononuclear phagocyte system (MPS), their poor stability biological fluids, premature release payload, low biocompatibility restricted clinical translation. In recent decades, chitosan (CS)-based nanodelivery systems (eg, polymeric NPs, micelles, liposomes, dendrimers, conjugates, solid lipid nanoparticles, etc.) attained promising from researchers improving pharmacokinetics pharmacodynamics chemotherapeutics. However, specialty this review mainly focus on critically discuss targeting potential various CS-based NPs treatment different types cancer. Based delivery mechanisms, we classified into stimuli-responsive, passive, or active nanosystems. Moreover, functionalization strategies grafting with polyethylene glycol (PEG), hydrophobic substitution, tethering stimuli-responsive linkers, conjugation ligands) adapted architecture CS-NPs target-specific chemotherapeutics also been considered. Nevertheless, based therapeutics hold great promise therapeutic outcomes while mitigating off-target effects chemotherapeutics, a long-term safety profile testing humans are warranted successful

Language: Английский

Citations

8

Nanodrugs based on co-delivery strategies to combat cisplatin resistance DOI
Qiubo Wang, Hui Li,

Wu Taixia

et al.

Journal of Controlled Release, Journal Year: 2024, Volume and Issue: 370, P. 14 - 42

Published: April 17, 2024

Language: Английский

Citations

7

Biopolymer-Based Nanomedicine for Cancer Therapy: Opportunities and Challenges DOI Creative Commons
Xixi Wu, Xin Yuan, Hengtong Zhang

et al.

International Journal of Nanomedicine, Journal Year: 2024, Volume and Issue: Volume 19, P. 7415 - 7471

Published: July 1, 2024

Abstract: Cancer, as the foremost challenge among human diseases, has plagued medical professionals for many years. While there have been numerous treatment approaches in clinical practice, they often cause additional harm to patients. The emergence of nanotechnology brought new directions cancer treatment, which can deliver anticancer drugs specifically tumor areas. This article first introduces application scenarios nanotherapies and strategies nanomedicine. Then, noteworthy characteristics exhibited by biopolymer materials were described, make biopolymers stand out polymeric nanomedicine delivery. Next, we focus on summarizing state-of-art studies five categories proteins (Albumin, Gelatin, Silk fibroin, Zein, Ferritin), nine varieties polysaccharides (Chitosan, Starch, Hyaluronic acid, Dextran, cellulose, Fucoidan, Carrageenan, Lignin, Pectin) liposomes field drug Finally, also provide a summary advantages limitations these biopolymers, discuss prevailing impediments their application, detail prospective research directions. review not only helps readers understand current development status nano delivery systems based but is helpful properties various find suitable solutions this through comparative reading. Keywords: delivery, nanoformulations, polymer, proteins,

Language: Английский

Citations

7

Advances in the delivery of anticancer drugs by nanoparticles and chitosan-based nanoparticles DOI Creative Commons

Prieložná Jarmila,

Veronika Mikušová, Peter Mikuš

et al.

International Journal of Pharmaceutics X, Journal Year: 2024, Volume and Issue: 8, P. 100281 - 100281

Published: Aug. 28, 2024

Cancer is the leading cause of death globally, and conventional treatments have limited efficacy with severe side effects. The use nanotechnology has potential to reduce effects drugs by creating efficient controlled anticancer drug delivery systems. Nanoparticles (NPs) used as carriers offer several advantages, including enhanced protection, biodistribution, selectivity and, pharmacokinetics. Therefore, this review devoted various organic (lipid, polymeric) well inorganic nanoparticles based on different building units providing a wide range potent Within these nanoparticulate systems, chitosan (CS)-based NPs are discussed particular emphasis due unique properties CS its derivatives non-toxicity, biodegradability, mucoadhesivity, tunable physico-chemical biological allowing their alteration specifically target cancer cells. In context streamlining systems (DDS), innovative nanoplatform-based therapy pathways involving passive active targeting stimuli-responsive DDS enhancing overall orthogonality developed NP-DDS towards included. most up-to-date information delivering anti-cancer using modern dosage forms specifically, CSNPs, summarised evaluated concerning benefits, limitations, advanced applications.

Language: Английский

Citations

7

Recent advances on chitosan/hyaluronic acid-based stimuli-responsive hydrogels and composites for cancer treatment: A comprehensive review DOI

Fahad Alsaikhan,

Bagher Farhood

International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: unknown, P. 135893 - 135893

Published: Sept. 1, 2024

Language: Английский

Citations

7

CD44 targeted delivery of oncolytic Newcastle disease virus encapsulated in thiolated chitosan for sustained release in cervical cancer: a targeted immunotherapy approach DOI Creative Commons
Kousain Kousar, Faiza Naseer, Maisa Siddiq Abduh

et al.

Frontiers in Immunology, Journal Year: 2023, Volume and Issue: 14

Published: May 22, 2023

Introduction Cervical cancer accounts for one of most common cancers among women reproductive age. Oncolytic virotherapy has emerged as a promising immunotherapy modality but it comes with several drawbacks that include rapid clearance virus from body due to immune-neutralization in host. To overcome this, we encapsulated oncolytic Newcastle disease (NDV) polymeric thiolated chitosan nanoparticles. For active targeting loaded nanoformulation against CD44 (cluster differentiation 44) receptors which are overly expressed on cells, these nanoparticles were surface functionalized hyaluronic acid (HA). Methods Using half dose NDV (TCID 50 (50% tissue culture infective dose) single 3 × 10 5 ), prepared by green synthesis approach through ionotropic gelation method. Zeta analysis was performed analyse size and charge Nanoparticles (NPs) shape analysed SEM (scanning electron microscope) TEM (transmission while functional group identification done FTIR (fourier transform infrared) XRD (X-ray diffraction). Viral quantification TCID Multiplicity infection (MOI) determination potential NPs MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay cell morphology analysis. Results showed average HA (HA-ThCs-NDV) 290.4nm zeta 22.3 mV 0.265 PDI (polydispersity index). smooth spherical features confirmed the presence characteristic groups successful encapsulation virus. In vitro release continuous sustained up 48 hours. HA-ThCs-NDV 2.63x 6 /mL titter exhibited high compared naked virus, dependent manner. Discussion These findings suggest functionalization is not only helpful achieving masking immune system but, also gives tumor microenvironment longer period time increases bioavailability

Language: Английский

Citations

15