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Scherersol delivery systems (Polysol / Quadrisol / Cosol)

✓ Approved

Cardinal Health, Inc. · 小分子 · 小分子

什么是 Scherersol delivery systems?

Scherersol delivery systems 是一种小分子,由Cardinal Health, Inc.研发。该药已获批,用于治疗相关适应症,给药途径:Oral (PO)。

药物档案

商品名Polysol, Quadrisol, Cosol
公司Cardinal Health, Inc.
药物类别小分子
给药途径Oral (PO)
状态Approved

治疗适应症

Scherersol delivery systems 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Surgical and medical proceduresOral appliance application✓ Approved

相关研究文献

PubMedGels (Basel, Switzerland)2026-10-26

Engineering Smart Hydrogels Through Dynamic Polymer Networks for Controlled Drug Delivery.

Choi Chanju C, Seo Dongseong D, Kim Taeho T, Park Jonghyun J et al.

Smart hydrogels are increasingly explored as adaptive platforms for controlled drug delivery because their polymer networks can respond dynamically to chemical, biological, and physical cues. Among these systems, dynamic polymer networks formed through reversible covalent and noncovalent interactions provide a unique means of coupling molecular-scale bond exchange with time-dependent changes in hydrogel structure, mechanics, degradation, and therapeutic transport. This review presents an integrated framework linking dynamic crosslink chemistry, exchange kinetics, network properties, and drug-release behavior. Dynamic covalent, supramolecular, metal-ligand, and hybrid network strategies are compared with particular emphasis on how crosslink lifetime, mesh accessibility, swelling, viscoelasticity, stress relaxation, and degradation govern therapeutic cargo loading, retention, diffusion, and release. Representative release mechanisms and kinetic models are discussed together with cargo-specific design considerations for small molecules, proteins and peptides, nucleic acids, and nanoparticle-based therapeutics. Biomedical applications are further considered according to therapeutic requirements and administration routes, including injectable local depots, topical and transdermal delivery, and regenerative systems. Finally, key translational challenges involving physiological complexity, biocompatibility, reproducibility, scale-up, sterilization, and storage stability are critically assessed. By connecting molecular interaction dynamics with network-level behavior and therapeutic performance, this review provides design principles for developing more predictable, programmable, and clinically translatable dynamic hydrogel drug-delivery systems.

PMID 42929917
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PubMedGels (Basel, Switzerland)2026-10-26

Hydrogel-Based Delivery Systems for Targeted Probiotic Release and Colonization: From Design Principles to Health Outcomes.

Yan Wenjia W, Shi Haichuan H, Wang Hao H, Xu Shanshan S et al.

Probiotics exert profound health benefits via the modulation of the intestinal microbiota. However, the efficacy of orally administered probiotics is severely constrained by a cascade of physiological barriers, including gastric acid inactivation, suboptimal intestinal release, and inadequate mucosal colonization. In response to these challenges, hydrogel-based delivery platforms have garnered considerable interest as versatile carriers capable of providing protective encapsulation, enabling spatiotemporally controlled release, and augmenting intestinal retention. This narrative review presents recent progress in the design and application of hydrogel-based oral delivery systems tailored for targeted probiotic release and effective colonization. First, the key gastrointestinal obstacles to successful probiotic delivery are delineated. Hydrogel design parameters are then critically appraised, with particular emphasis on material selection and network design. The underlying release mechanisms are subsequently examined. These encompass pH-responsive, enzyme-triggered, and inflammation-responsive modalities. Emerging colonization-enhancing strategies are discussed in detail. These include mucoadhesive hydrogel architectures and the nascent paradigm of "living hydrogels" functioning as dynamic bioreactors. The translational potential of these systems for health management is illustrated through applications in inflammatory bowel disease, colorectal cancer, and gut-brain axis modulation. Finally, key challenges in manufacturing, viability, and translational feasibility are evaluated. These include regulatory, safety, and encapsulation-related constraints. To address these, multi-responsive platforms, machine learning-assisted design, and synbiotic hydrogels are proposed. These hydrogels synergize with probiotics to target dysbiosis and repair mucosal damage for improved gastrointestinal health management.

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PubMedBiomimetics (Basel, Switzerland)2026-10-26

Inkjet and Related Printing Technologies for Plant Systems: From Physiological Monitoring to Functional Biofabrication.

Wang Xiukun X, Zhang Xing X, Wang Guanghui G, Feng Bokai B et al.

Featuring non-contact, high-precision, and multi-material deposition, inkjet and related printing technologies offer a new alternative technique for plant systems. However, the spatial heterogeneity, continuous growth, and sensitivity of plant tissues to external perturbations make it difficult for conventional methods to target specific sites on living organs. This review evaluates thermal and piezoelectric inkjet printing, together with aerosol jet and electrohydrodynamic printing for plant applications. Moreover, it relates the jetting behavior of the printhead to interfacial processes between droplets and plant surfaces. Practical performance is assessed across four dimensions: effective feature size, organ-scale throughput, potential biological damage, and the physiological compatibility of printing inks with plants. Applications are then organized within a framework comprising five tiers: monitoring, delivery, sensing, biofabrication, and intelligent systems. Specifically, recent studies have demonstrated that these printing approaches can be employed for surface labeling and growth tracking of plant organs, localized delivery of agricultural inputs, fabrication of flexible sensors, and construction of living materials (e.g., plant cells). Combined with artificial intelligence technology, these capabilities could form a closed-loop system spanning sensing to feedback, with printing as the precision actuator, potentially shifting plant management from passive observation to active regulation. Finally, this review discusses the challenges of living-interface dynamics, ink biocompatibility, multiscale integration, and data intelligence. It further outlines the prospects of these technologies for programmable plants and living agricultural interfaces. By bridging printing technologies, plant systems, and functional biofabrication, this review provides a unified framework to guide the development of intelligent and sustainable agricultural systems.

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PubMedBiosensors2026-10-26

Hypoxia-Responsive Fluorescent Prodrugs: Self-Reporting Drug Delivery or Activation in Living Systems.

Hu Xiaomu X, Song Xiaoyu X, Qiu Yijie Y, Du Wei W

Hypoxia is a hallmark of numerous pathological conditions, such as cancer, drug-induced liver injury, and rheumatoid arthritis. Given the contrast in oxygen levels between pathological and normal tissues, hypoxia-activated prodrugs have been developed by incorporating hypoxia-responsive groups to achieve targeted therapy while minimizing toxicity to normal cells. Recently, the integration of drug delivery or activation (including triggered release) with fluorescence imaging has emerged as a promising strategy in prodrug design, enabling self-reporting of drug processes and facilitating preclinical evaluation of prodrug performance. This review provides a comprehensive overview of hypoxia-responsive fluorescent prodrugs capable of self-reporting drug delivery or activation/release via fluorescence readouts. We summarize recent advancements in such prodrugs, focusing on design strategies, drug release or activation mechanisms, fluorescence signal modulation, and biomedical applications, especially in cancer treatment. Furthermore, we discuss current challenges and future perspectives for hypoxia-responsive fluorescent prodrugs, as well as potential directions for the development of the next generation of hypoxia-responsive prodrugs.

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PubMedBMC proceedings2026-10-26

Meeting report of the fifth symposium organized by the coalition to strengthen the HPV immunization community (CHIC): Nairobi, Kenya - advancing sustainable HPV vaccination programs in Africa.

Bolio Ana A, Jennings Mary Carol MC, Burdier Ricardo R, Jindal Sakshi S et al.

HPV vaccination coverage across Africa has improved substantially in recent years but remains below elimination thresholds, with persistent gaps in reaching hard-to-reach populations and growing uncertainty around future financing. This report summarizes proceedings from the fifth regional symposium of the Coalition to Strengthen the HPV Immunization Community (CHIC), held in Nairobi, Kenya, in October 2025 in collaboration with Kenya's Ministry of Health. The three-day symposium convened over 100 participants from 22 African countries, including national immunisation program managers, ministry officials, researchers, civil society representatives, and global partners (WHO, UNICEF, Gavi, PATH, the Gates Foundation). The agenda, developed through stakeholder interviews and prior scientific and advisory input, centered on six subthemes related to program sustainability. Plenary sessions addressed epidemiological trends, national policy updates including Kenya's transition to a single-dose schedule, and implications of Gavi's upcoming consolidated funding model (Gavi 6.0). Country snapshot presentations and service-delivery case studies facilitated cross-country peer learning. On day three, though an electronic poll of helped to prioritize 12 candidate implementation themes, which structured subsequent round table working groups. Countries then developed individual action plans identifying priority challenges, responsible stakeholders, and implementation timelines. Sustainable service delivery, financing, and data systems emerged as the highest-priority implementation themes. Country action plans most frequently targeted data systems strengthening, communication and community engagement, sustainable service delivery, and financing mechanisms, with additional attention to service integration, hard-to-reach populations, and target population expansion. Cross-cutting synthesis identified recurring concerns regarding HPV vaccination for people living with HIV, fragmented data systems, the role of program integration, financing sustainability under evolving donor models, and underrecognized risks from misinformation, including emerging AI-generated content. The symposium reinforced CHIC's role as a platform for peer-to-peer learning across countries at varying stages of HPV vaccine introduction, surfacing shared structural barriers to sustainability alongside country-specific action plans. Findings underscore the need for sustained political commitment, financing transition planning, digital system strengthening, and multisectoral integration to support the WHO goal of cervical cancer elimination by 2030.

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PubMedGels (Basel, Switzerland)2026-10-26

Stimuli-Responsive Hydrogels for Oral Probiotic Delivery: Balancing Protection and Site-Specific Release.

Jung Sungwon S, Noh Sookyung S, Lee Hyeonseung H, Park Sohyeon S

Successful oral probiotic delivery requires protection of viable cells during gastrointestinal transit followed by efficient release at the target intestinal site. Stimuli-responsive hydrogels can provide both functions, although network properties that restrict acid, bile, and enzyme transport may also delay the structural changes required for release. This review discusses how crosslink density, particle geometry, the internal microenvironment, and interfacial layers shape this protection-release relationship. pH-, enzyme/microbiota-, redox-, and multi-stimuli-responsive systems are compared with emphasis on the structural changes that allow bacterial escape. Because probiotic cells are much larger than the molecular mesh of most hydrogels, release generally requires network opening through swelling, formation or enlargement of cell-scale pores or defects, erosion, fracture, de-crosslinking, or dissolution rather than ordinary molecular diffusion. Delivery performance should therefore be evaluated using release kinetics, viability of released cells, retained cells, and total viable recovery in sequential gastrointestinal models. Strain-specific testing, storage studies, and in vivo validation will also be important. The practical goal is a reproducible protection-release window that maintains cell viability without delaying release.

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