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Phthalocyanines are ideal candidates as photosensitizers for photodynamic therapy (PDT) of cancer due to their favorable chemical and photophysical properties. However, their tendency to form aggregates in water reduces PDT efficacy and poses challenges in obtaining efficient forms of phthalocyanines for therapeutic applications. In the current work, polyvinylpyrrolidone (PVP) and micellar formulations were compared for encapsulating and monomerizing a water-soluble zinc phthalocyanine bearing four non-peripheral triethylene glycol chains (). H NMR spectroscopy combined with UV-vis absorption and fluorescence spectroscopy revealed that exists as a mixture of regioisomers in monomeric form in dimethyl sulfoxide but forms dimers in an aqueous buffer. PVP, polyethylene glycol castor oil (Kolliphor RH40), and three different triblock copolymers with varying proportions of polyethylene and polypropylene glycol units (termed P188, P84, and F127) were tested as micellar carriers for . H NMR chemical shift analysis, diffusion-ordered spectroscopy, and 2D nuclear Overhauser enhancement spectroscopy was applied to monitor the encapsulation and localization of at the polymer interface. Kolliphor RH40 and F127 micelles exhibited the highest affinity for encapsulating in the micellar core and resulted in intense fluorescence emission as well as efficient singlet oxygen formation along with PVP. Among the triblock copolymers, efficiency in binding and dimer dissolution decreased in the order F127 > P84 > P188. PVP was a strong binder for . However, molecules are rather surface-attached and exist as monomer and dimer mixtures. The results demonstrate that NMR combined with optical spectroscopy offer powerful tools to assess parameters like drug binding, localization sites, and dynamic properties that play key roles in achieving high host-guest compatibility. With the corresponding adjustments, polymeric micelles can offer simple and easily accessible drug delivery systems optimizing phthalocyanines' properties as efficient photosensitizers.
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http://dx.doi.org/10.1021/acs.molpharmaceut.3c00306 | DOI Listing |
Colloids Surf B Biointerfaces
August 2025
CNR - Institute of Biomolecular Chemistry, Via Paolo Gaifami 18, Catania 95126, Italy. Electronic address:
Iodine is the most potent antiseptic agent used in clinical applications, but its volatility and toxicity are serious drawbacks that are stimulating the search of new strategies to achieve formulations stable at low iodine concentration. Here, we report that polycationic micellar aggregates, formed by the self-assembling of the amphiphilic choline-calix[4]arene derivative (CholCalix) in aqueous medium, are able to complex triiodide anions (I) both in solution and in solid phase. This novel iodophor enhances the stability of 0.
View Article and Find Full Text PDFInvest New Drugs
September 2025
Department of Pharmaceutics, Sri Adichunchanagiri College of Pharmacy, Adichunchanagiri University, BG Nagar, 571448, Karnataka, India.
Multidrug resistance (MDR) appears to be a major challenge in cancer treatment, frequently leading to suboptimal clinical results and treatment failure. A transmembrane efflux pump called P-glycoprotein (P-gp) is essential to multidrug resistance because it actively transports various chemotherapeutic drugs out of cancer cells, lowering their intracellular concentrations and efficacy. To improve treatment approaches, it is essential to comprehend the structural and functional dynamics of P-glycoprotein and the genetic and epigenetic processes controlling its expression.
View Article and Find Full Text PDFPharmaceutics
July 2025
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
: Paclitaxel (PTX) is widely used in the treatment of a variety of solid tumours due to its broad-spectrum anti-tumour activity, but its use in brain gliomas is limited by insufficient blood-brain tumour barrier (BBTB) penetration and systemic toxicity. The aim of this study was to develop a Solutol HS-15-based micellar nanoparticle (PSM) to enhance the brain glioma targeting of PTX and reduce toxicity. : PSMs were prepared by solvent injection and characterised for particle size, encapsulation rate, haemolysis rate and in vitro release properties.
View Article and Find Full Text PDFJ Control Release
August 2025
School of Pharmacy, Queen's University Belfast, UK. Electronic address:
Lipid-based nanocarrier systems have multiple advantages, including biocompatibility, biodegradability and drug loading capacity. Combining these findings with the concept of dissolving microneedles (MNs) would aid in the efficient delivery of peptides and improve therapeutic outcomes. Thus, MN-mediated transdermal delivery was explored for the delivery of salmon calcitonin (sCT).
View Article and Find Full Text PDFColloids Surf B Biointerfaces
August 2025
Department of Biology and Chemistry, Texas A&M International University, Laredo, TX 78041, United States. Electronic address:
Surfactants are essential ingredients in detergents and personal care products due to their ability to emulsify oils, lower surface tension, and facilitate cleansing. However, increasing evidence links surfactant exposure to adverse effects on human skin, such as lipid disruption, protein denaturation, and inflammatory responses. This review synthesizes recent interdisciplinary research on surfactant chemistry, critical micelle concentration (CMC), and dermal interactions, with a particular focus on their biophysical behavior, cytotoxicity, and irritation potential.
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