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Micro/Nanomaterials-Augmented Hydrogen Therapy.

マイクロ・ナノ材料を活用した水素医療の増強戦略に関するレビュー

review mixed routes not assessed

Abstract

Molecular hydrogen exhibits bio-reductive and homeostatic properties that confer beneficial effects against oxidative stress- and inflammation-related conditions. Unlike gaseous transmitters such as NO, CO, and H2S, H2 does not interfere with oxygen transport by erythrocytes, making high-concentration exposure relatively safe. However, its low aqueous solubility and non-directional diffusion limit site-specific efficacy. This review introduces the concept of hydrogen nanomedicine, systematically organizing approaches that employ functional micro/nanomaterials to achieve targeted hydrogen delivery, controlled release, and nanocatalytic or multimodal enhancement of hydrogen efficacy. These strategies are presented as a framework for advancing the investigation of hydrogen's effects on inflammation-related diseases.

Mechanism

H2 exerts bio-reductive effects and modulates homeostatic pathways to suppress oxidative stress and inflammation. Functional micro/nanomaterials enable targeted delivery and controlled release, increasing local H2 concentration and enhancing efficacy at disease sites.

Bibliographic

Authors
Zhou G, Goshi E, He Q
Journal
Adv Healthc Mater
Year
2019
PMID
31267691
DOI
10.1002/adhm.201900463

Tags

Delivery:点滴投与 Mechanism:抗酸化酵素 ヒドロキシルラジカル消去 炎症抑制 ミトコンドリア 酸化ストレス 活性酸素種

Delivery context

This study combines multiple delivery routes. As a general principle, the most efficient route for routine hydrogen intake is inhalation. Inhalation carries explosion risk (empirical LFL of 10%; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

Safety notes

This study combines multiple delivery routes. As a general principle, the most efficient route for routine hydrogen intake is inhalation. Inhalation carries explosion risk (empirical LFL of 10%; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

See also:

Cite as: H2 Papers — PMID 31267691. https://h2-papers.org/en/papers/31267691
Source: PubMed PMID 31267691