Venom-loaded cationic-functionalized poly(lactic acid) nanoparticles for serum production against Tityus serrulatus scorpion

• Philippe de Castro Mesquita,
• Karla Samara Rocha Soares,
• Manoela Torres-Rêgo,
• Emanuell dos Santos-Silva,
• Mariana Farias Alves-Silva,
• Alianda Maira Cornélio,
• Matheus de Freitas Fernandes-Pedrosa and
• Arnóbio Antônio da Silva-Júnior

Beilstein J. Nanotechnol. 2025, 16, 1633–1643, doi:10.3762/bjnano.16.115

• nanoparticles had the same response when compared with that of AH standard formulation [11]. Cationic PLA nanoparticles produced in this study demonstrated better immune stimulation behavior. These results can be found in other chitosan-based cationic nanoparticle formulations [1][45]. The cationic properties

Atomic-level characterization and cilostazol affinity of poly(lactic acid) nanoparticles conjugated with differentially charged hydrophilic molecules

• María Francisca Matus,
• Martín Ludueña,
• Cristian Vilos,
• Iván Palomo and
• Marcelo M. Mariscal

Beilstein J. Nanotechnol. 2018, 9, 1328–1338, doi:10.3762/bjnano.9.126

• green-styled lines. Distances between NH2 groups from a cationic nanoparticle and the center of mass of the PLA core are represented in ten different blue-styled lines. Interaction energy (kcal/mol) between the PLA core and DSPE–PEG lipid portion. Ten lowest computed binding energy values for cilostazol

Cationic PEGylated polycaprolactone nanoparticles carrying post-operation docetaxel for glioma treatment

• Cem Varan and
• Erem Bilensoy

Beilstein J. Nanotechnol. 2017, 8, 1446–1456, doi:10.3762/bjnano.8.144

• suggested to result in a more effective brain tumor treatment when compared to chemotherapeutics administered as an intravenous bolus infusion. Keywords: bioadhesive film; cationic nanoparticle; core–shell nanoparticle; docetaxel; glioma; Introduction A brain tumor is known as an abnormal growth of

• administration for therapeutic nanoparticles help reduce systemic side effects, bypass BBB and improve efficacy of the drug by forming a constant drug reservoir directly at target site [43][44][45][46][47][48][49]. The goal of this study was to evaluate and characterize implantable cationic nanoparticle-loaded