Cholesterol‐Conjugated PAMAM Dendrimers: Enhancing Stability, Drug Delivery Efficiency, and In Vitro Anticancer Performance DOI Open Access
Ngoc Luu,

Hung Q. Ly,

Chinh Van Nguyen

и другие.

Journal of Polymer Science, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 24, 2024

ABSTRACT Nanomaterials offer great potential in cancer treatment, particularly drug delivery, where their unique properties allow for targeted therapy, increasing treatment efficacy while minimizing side effects. Dendrimers, with highly branched structure, are ideal candidates delivery. However, polyamidoamine (PAMAM) dendrimers, despite versatility, exhibit cytotoxicity. Modifying PAMAM dendrimers cholesterol through p‐nitrophenyl chloroformate (NPC) mediation enhances biocompatibility and targeting ability, especially toward cells. In this study, G3.0 was successfully synthesized conjugated to form G3C nanogels, a nanoscale size of 83.8 ± 21.9 nm. The study conjugation revealed that at 25% surface functionalization G3.0, exhibited stable behavior PBS buffer up 8 days. system's capacity load single or dual drugs also explored, demonstrating controlled release over 96 h. Moreover, modification on significantly enhanced cell compatibility. G3C@QU/PTX system improved HeLa cells vitro compared healthy fibroblast This research provides strong foundation developing nanomaterials treatment.

Язык: Английский

Advances in Mesoporous Silica Nanoparticles as Carriers for Drug Delivery and other Biomedical Applications DOI

Grini Mohammed Ilyes,

Benbayer Chahinez,

Salima Saïdi‐Besbes

и другие.

Microporous and Mesoporous Materials, Год журнала: 2025, Номер unknown, С. 113603 - 113603

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

3

Longan-inspired chitosan-pectin core-shell hydrogel beads for oral delivery of biodrugs to enhance osteoporosis therapy DOI Creative Commons
V.H. Giang Phan, Bich-Phuong Thi Nguyen, Thi Yen Nhi Nguyen

и другие.

International Journal of Biological Macromolecules, Год журнала: 2025, Номер unknown, С. 142254 - 142254

Опубликована: Март 1, 2025

Osteoporosis, a common disorder, is characterized by systemic reduction in bone mass and structural integrity, resulting brittle bones. Reducing loss enhancing density through oral administration of biopharmaceuticals provides significant advantages, including convenience non-invasiveness for patients. However, challenges such as poor absorption enzymatic degradation necessitate the development innovative drug delivery systems. This research introduces core-shell hydrogel system inspired natural architecture Longan fruit, constructed from pectin chitosan biopolymers, designed to create biocapsules sustain release biodrugs. In this system, salmon calcitonin (sCT) was encapsulated within mesoporous silica nanoparticles (MSNs) incorporated into core beads. The synthesis beads carefully regulated adjusting immersion time concentration crosslinker. demonstrated durability, with shell effectively preventing rapid stomach, while layer enhanced adhesion intestinal walls, safeguarded sCT, enabled sustained over an extended period up 30 h. Furthermore, biocompatibility tests indicated minimal cytotoxicity hemolysis. Cellular uptake assays that sCT ensured its prolonged CT-26 cells. study presents promising platform delivery, offering efficacy, patient compliance, potential replacement injection-based therapies.

Язык: Английский

Процитировано

1

Mineralized Biopolymers‐Based Scaffold Encapsulating with Dual Drugs for Alveolar Ridge Preservation DOI Open Access

Thanh‐Han Hoang Tran,

Cuong Hung Luu, Kien T. Nguyen

и другие.

Macromolecular Bioscience, Год журнала: 2024, Номер unknown

Опубликована: Окт. 15, 2024

Abstract Mineralization of scaffolds is essential for alveolar ridge preservation and bone tissue engineering, enhancing the mechanical strength bioactivity scaffolds, promoting better integration with natural tissue. While in situ mineralization method using concentrated SBF solutions promising, there limited comprehensive research on its effects. In this study, it demonstrate that soaking gelatin/alginate (GAS) fivefold significantly reduces time to 3–7 days but also leads considerable degradation loss scaffold's original microstructure. The ratio gelatin alginate optimized improve properties GAS. GAS sample, when soaked form GAS/HAp, exhibited hydroxyapatite (HAp) crystal formation starting from day 3, mature hexagonal crystals forming by 7. However, process caused significant decomposition deformation pore structure. Additionally, biocompatibility GAS/HAp evaluated through vitro, ovo, haemolysis, anti‐ROS assays. findings highlight impact 5× GAS, laying groundwork further engineering.

Язык: Английский

Процитировано

4

pH- and redox-sensitive selenium-incorporated mesoporous silica nanoparticles for osteosarcoma-targeted treatment DOI Creative Commons
Le He,

Zahra Javid Anbardan,

Pamela Habibović

и другие.

Materials & Design, Год журнала: 2025, Номер unknown, С. 113883 - 113883

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Biocompatible Materials for Light Emitters DOI
Saheed Abiola Raheem, Olayinka Oderinde

Engineering materials, Год журнала: 2025, Номер unknown, С. 65 - 72

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Dual-functional injectable hydrogel as antimicrobial and angiogenic therapeutics for dental pulp regeneration DOI
Nhu Nguyen, Cuong Hung Luu,

Ngoc-Dan Ho Nguyen

и другие.

Journal of Materials Chemistry B, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Development of an injectable polysaccharide-based hydrogel system with antibacterial and angiogenic properties for pulpitis treatment.

Язык: Английский

Процитировано

0

Development and Characterization of Folic Acid‐Decorated Fucoidan‐Poloxamer 407 Self‐Assembled Nanogels Co‐Loading Curcumin and Paclitaxel for Synergistically Enhanced Chemotherapeutic Efficacy DOI
Ngoc The Nguyen, Cuong Hung Luu,

Anh Quan Hoang

и другие.

Journal of Polymer Science, Год журнала: 2025, Номер unknown

Опубликована: Май 5, 2025

ABSTRACT Cancer‐targeted nanomedicines demonstrate considerable potential in anticancer treatment due to their unique properties that improve therapeutic efficiency while minimizing off‐target effects. In this research, curcumin (Cur) and paclitaxel (PTX) were co‐loaded into dual‐targeting folate receptor/P‐selectin nanocarriers, which based on folate‐conjugated fucoidan‐poloxamer 407 copolymers (FA‐FP407), aiming inhibit breast cancer through intravenous administration. The successful synthesis of the self‐assembled nanogels was confirmed by analyzing chemical composition. resulting exhibited optimal physicochemical properties, including a negative surface charge, spherical morphology, hydrodynamic diameter 158.27 ± 3.15 nm, along with high drug‐loading efficiency. vitro drug release from significantly accelerated within tumor microenvironment at pH 5.5, it slowed down under physiological conditions. kinetics adhered Fickian diffusion model. Additionally, blank nanocarriers both hemocompatible cytocompatible, although they slight growth inhibition MCF‐7 cells. FA‐FP407@Cur@PTX demonstrated lower IC 50 compared free formulations single drug‐loaded cells, indicating could enhance activity co‐administering different drugs precisely accumulating cancerous site. This effect is attributed strong synergistic actions receptor‐mediated cellular uptake. study provides solid foundation for advancing targeted nanomedicine, facilitating co‐delivery multiple agents achieve superior effects chemotherapy.

Язык: Английский

Процитировано

0

Cholesterol‐Conjugated PAMAM Dendrimers: Enhancing Stability, Drug Delivery Efficiency, and In Vitro Anticancer Performance DOI Open Access
Ngoc Luu,

Hung Q. Ly,

Chinh Van Nguyen

и другие.

Journal of Polymer Science, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 24, 2024

ABSTRACT Nanomaterials offer great potential in cancer treatment, particularly drug delivery, where their unique properties allow for targeted therapy, increasing treatment efficacy while minimizing side effects. Dendrimers, with highly branched structure, are ideal candidates delivery. However, polyamidoamine (PAMAM) dendrimers, despite versatility, exhibit cytotoxicity. Modifying PAMAM dendrimers cholesterol through p‐nitrophenyl chloroformate (NPC) mediation enhances biocompatibility and targeting ability, especially toward cells. In this study, G3.0 was successfully synthesized conjugated to form G3C nanogels, a nanoscale size of 83.8 ± 21.9 nm. The study conjugation revealed that at 25% surface functionalization G3.0, exhibited stable behavior PBS buffer up 8 days. system's capacity load single or dual drugs also explored, demonstrating controlled release over 96 h. Moreover, modification on significantly enhanced cell compatibility. G3C@QU/PTX system improved HeLa cells vitro compared healthy fibroblast This research provides strong foundation developing nanomaterials treatment.

Язык: Английский

Процитировано

3