Natural endogenous material-based vehicles for delivery of macromolecular drugs DOI
Lu An, Kang Du, Meng Wang

et al.

Chinese Journal of Natural Medicines, Journal Year: 2024, Volume and Issue: 22(12), P. 1163 - 1176

Published: Dec. 1, 2024

Language: Английский

Thermosensitive hydrogel with emodin-loaded triple-targeted nanoparticles for a rectal drug delivery system in the treatment of chronic non-bacterial prostatitis DOI Creative Commons
Yan Ye,

Wenzhen Zhong,

Ruifeng Luo

et al.

Journal of Nanobiotechnology, Journal Year: 2024, Volume and Issue: 22(1)

Published: Jan. 18, 2024

Abstract Background The complex etiology and pathogenesis underlying Chronic Non-Bacterial Prostatitis (CNP), coupled with the existence of a Blood Prostate Barrier (BPB), contribute to lack specificity poor penetration most drugs. Emodin (EMO), potential natural compound for CNP treatment, exhibits commendable anti-inflammatory, anti-oxidant, anti-fibrosis properties but suffers from same problems as other Methods By exploiting recognition lactoferrin (LF) receptors that target intestinal epithelial cells (NCM-460) prostate (RWPE-1), pathway is established transrectal absorption EMO effectively reach prostate. Additionally, hyaluronic acid (HA) employed, recognizing CD44 which macrophages within inflamed This interaction facilitates intraprostatic delivery EMO, leading its pronounced anti-inflammatory effects. A thermosensitive hydrogel (CS-Gel) prepared chitosan (CS) β-glycerophosphate disodium salt (β-GP) was used rectal drug strong adhesion achieve effective retention sustained slow release. Thus, we developed triple-targeted nanoparticle (NPs)/thermosensitive (Gel) system. In this process, LF, positive charge, utilized load through dialysis, producing LF@EMO-NPs. Subsequently, HA employed encapsulate EMO-loaded LF nanoparticles via electrostatic adsorption, yielding HA/LF@EMO-NPs. Finally, HA/LF@EMO-NPs lyophilized powder added CS-Gel (HA/LF@EMO-NPs Gel). Results Cellular assays indicated NCM-460 RWPE-1 showed high uptake both LF@EMO-NPs HA/LF@EMO-NPs, while Raw 264.7 exhibited substantial For LPS-induced cells, can reduce inflammatory responses by modulating TLR4/NF-κB signaling pathways. Tissue imaging corroborated capacity HA/LF-modified formulations breach BPB, accumulating gland's lumen. Animal experiments administration Gel significantly reduced cytokine expression, oxidative stress levels fibrosis in rats, addition exerting effects inhibiting NF-κB without obvious toxicity. Conclusion NPs/Gel system slow-release shows great treatment CNP. Graphical

Language: Английский

Citations

18

Cell Membrane-Coated Biomimetic Nanoparticles in Cancer Treatment DOI Creative Commons
Shu Zhang, Xiaojuan Zhang, Huan Gao

et al.

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(4), P. 531 - 531

Published: April 12, 2024

Nanoparticle-based drug delivery systems hold promise for cancer treatment by enhancing the solubility and stability of anti-tumor drugs. Nonetheless, challenges inadequate targeting limited biocompatibility persist. In recent years, cell membrane nano-biomimetic have emerged as a focal point research development, due to their exceptional traits, including precise targeting, low toxicity, good biocompatibility. This review outlines categorization advantages bionic nano-delivery systems, provides an introduction preparation methods, assesses applications in treatment, chemotherapy, gene therapy, immunotherapy, photodynamic photothermal combination therapy. Notably, delves into application various identifies opportunities future advancement. Embracing membrane-coated biomimetic nanoparticles presents novel unparalleled avenue personalized tumor

Language: Английский

Citations

18

Multifunctional engineered mesoporous silica/inorganic material hybrid nanoparticles: Theranostic perspectives DOI

Neha Benedicta Fernandes,

Yogendra Nayak, Sanjay Garg

et al.

Coordination Chemistry Reviews, Journal Year: 2022, Volume and Issue: 478, P. 214977 - 214977

Published: Dec. 15, 2022

Language: Английский

Citations

58

Cell membrane-camouflaged bufalin targets NOD2 and overcomes multidrug resistance in pancreatic cancer DOI Creative Commons
Wei Zhang,

Yibao Fan,

Jinze Zhang

et al.

Drug Resistance Updates, Journal Year: 2023, Volume and Issue: 71, P. 101005 - 101005

Published: Aug. 21, 2023

Multidrug resistance in pancreatic cancer poses a significant challenge clinical treatment. Bufalin (BA), compound found secretions from the glands of toads, may help overcome this problem. However, severe cardiotoxicity thus far has hindered its application. Hence, present study aimed to develop cell membrane-camouflaged and BA-loaded polylactic-co-glycolic acid nanoparticle (CBAP) assess potential counter chemoresistance cancer.The toxicity CBAP was evaluated by electrocardiogram, body weight, distress score, nesting behavior mice. In addition, anticarcinoma activity underlying mechanism were investigated both vitro vivo.CBAP significantly mitigated BA-mediated acute enhanced sensitivity several drugs, such as gemcitabine, 5-fluorouracil, FOLFIRINOX. Mechanistically, directly bound nucleotide-binding oligomerization domain containing protein 2 (NOD2) inhibited expression nuclear factor kappa-light-chain-enhancer activated B cells. This inhibits ATP-binding cassette transporters, which are responsible for cells.Our findings indicate that NOD2. Combining with standard-of-care chemotherapeutics represents safe efficient strategy treatment cancer.

Language: Английский

Citations

30

“Hook&Loop” multivalent interactions based on disk-shaped nanoparticles strengthen active targeting DOI

Ni Dong,

Zhenyun Liu,

Haisheng He

et al.

Journal of Controlled Release, Journal Year: 2023, Volume and Issue: 354, P. 279 - 293

Published: Jan. 12, 2023

Language: Английский

Citations

24

A Review: Surface Engineering of Lipid‐Based Drug Delivery Systems DOI Creative Commons
Dhaval Patel, Jyoti Solanki, Mafatlal M. Kher

et al.

Small, Journal Year: 2024, Volume and Issue: 20(43)

Published: July 14, 2024

This review explores the evolution of lipid-based nanoparticles (LBNPs) for drug delivery (DD). Herein, LBNPs are classified into liposomes and cell membrane-based (CMNPs), each with unique advantages challenges. Conventional possess drawbacks such as poor targeting, quick clearance, limited biocompatibility. One possible alternatives to overcome these challenges is surface modification (NPs) materials polyethylene glycol (PEG), aptamers, antibody fragments, peptides, CD44, hyaluronic acid, folic palmitic lactoferrin. Thus, main focus this will be on different modifications that enable have beneficial properties DD, enhancing mass transport properties, immune evasion, improved stability, targeting. Moreover, various CMNPs explored used DD derived from cells red blood (RBCs), platelets, leukocytes, cancer cells, stem highlighting their natural (e.g., biocompatibility ability evade system). discussion extends biomimicking hybrid NPs accomplished through coating synthetic (mainly polymeric) membranes. aims provide a comprehensive resource researchers recent advances in field CMNPs. Overall, provides valuable insights dynamic systems.

Language: Английский

Citations

16

Endoplasmic reticulum-targeted delivery of celastrol and PD-L1 siRNA for reinforcing immunogenic cell death and potentiating cancer immunotherapy DOI Creative Commons
Jie Wang, Zilong Zhang, Yan Zhuo

et al.

Acta Pharmaceutica Sinica B, Journal Year: 2024, Volume and Issue: 14(8), P. 3643 - 3660

Published: April 15, 2024

The prospect of employing chemoimmunotherapy targeted towards the endoplasmic reticulum (ER) presents an opportunity to amplify synergistic effects chemotherapy and immunotherapy. In this study, we initially validated celastrol (CEL) as inducer immunogenic cell death (ICD) by promoting ER stress autophagy in colorectal cancer (CRC) cells. Subsequently, ER-targeted strategy was posited, involving codelivery CEL with PD-L1 small interfering RNAs (siRNA) using KDEL peptide-modified exosomes derived from milk (KME), enhance outcomes. Our findings demonstrate efficient transportation KME via Golgi-to-ER pathway. Compared their non-targeting counterparts, exhibited a significant augmentation CEL-induced ICD effect. Additionally, it facilitated release danger signaling molecules (DAMPs), thereby stimulating antigen-presenting function dendritic cells infiltration T into tumor. Concurrently, delivery siRNA resulted downregulation both intracellular membrane protein expression, consequently fostering proliferation activity CD8+ Ultimately, formulation enhanced anti-tumor efficacy provoked immune responses against orthotopic tumors vivo. Collectively, robust provides encouraging approach for achieving potent chemoimmunotherapy.

Language: Английский

Citations

11

Engineered Cell Membrane-Camouflaged Nanomaterials for Biomedical Applications DOI Creative Commons
Xiaoxuan Guan, Simin Xing, Yang Liu

et al.

Nanomaterials, Journal Year: 2024, Volume and Issue: 14(5), P. 413 - 413

Published: Feb. 23, 2024

Recent strides in nanomaterials science have paved the way for creation of reliable, effective, highly accurate, and user-friendly biomedical systems. Pioneering integration natural cell membranes into sophisticated nanocarrier architectures, membrane camouflage has emerged as a transformative approach regulated drug delivery, offering benefits minimal immunogenicity coupled with active targeting capabilities. Nevertheless, utility such is curtailed by challenges like suboptimal precision lackluster therapeutic efficacy. Tailored engineering stands at forefront biomedicine, equipping nanoplatforms capacity to conduct more complex operations. This review commences an examination prevailing methodologies engineering, spotlighting strategies direct chemical modification, lipid insertion, hybridization, metabolic glycan labeling, genetic engineering. Following this, evaluation unique attributes various presented, delivering in-depth scrutiny substantial advancements applications driven cutting-edge engineered camouflage. The discourse culminates recapitulating salient influence within nanomaterial prognosticates its seminal role healthcare technologies. It envisaged that insights offered herein will catalyze novel avenues innovation refinement camouflaged nanotechnologies.

Language: Английский

Citations

10

Nanoparticles exhibiting virus-mimic surface topology for enhanced oral delivery DOI Creative Commons

Zhentao Sang,

Lu Xu, Renyu Ding

et al.

Nature Communications, Journal Year: 2023, Volume and Issue: 14(1)

Published: Nov. 24, 2023

The oral delivery of nano-drug systems (Nano-DDS) remains a challenge. Taking inspirations from viruses, here we construct core-shell mesoporous silica nanoparticles (NPs, ~80 nm) with virus-like nanospikes (VSN) to simulate viral morphology, and further modified VSN L-alanine (CVSN) enable chiral recognition for functional bionics. By comparing the solid NPs, NPs VSN, demonstrate advantages CVSN on overcoming intestinal sequential barriers in both animals human via multiple biological processes. Subsequently, encapsulate indomethacin (IMC) into nanopores mimic gene package, wherein payloads are isolated bio-environments exist an amorphous form increase their stability solubility, while multi-sited anchor recognize mucosa enhance penetrability ultimately improve adsorption IMC. Encouragingly, also prove versatility as Nano-DDS.

Language: Английский

Citations

22

Morphology-Dependent Interaction of Silica Nanoparticles with Intestinal Cells: Connecting Shape to Barrier Function DOI Creative Commons
Claudia Iriarte‐Mesa, Maximilian Jobst, Janice Bergen

et al.

Nano Letters, Journal Year: 2023, Volume and Issue: 23(16), P. 7758 - 7766

Published: July 11, 2023

The intestinal compartment ensures nutrient absorption and barrier function against pathogens. Despite decades of research on the complexity gut, adaptive potential to physical cues, such as those derived from interaction with particles different shapes, remains less understood. Taking advantage technological versatility silica nanoparticles, spherical, rod-shaped, virus-like materials were synthesized. Morphology-dependent interactions studied differentiated Caco-2/HT29-MTX-E12 cells. Contributions shape, aspect ratio, surface roughness, size evaluated considering influence mucus layer intracellular uptake pathways. Small particle roughness favored highest penetration through but limited cell monolayer efficient internalization. Particles a larger ratio (rod-shaped) seemed privilege paracellular permeation increased cell–cell distances, albeit without hampering integrity. Inhibition clathrin-mediated endocytosis chemical modulation junctions effectively tuned these responses, confirming morphology-specific elicited by bioinspired nanomaterials.

Language: Английский

Citations

16