核心型纳米剂通过基诱导和氧化物增强的氧化损伤使光触发的协同抗瘤活性成为可能
Qun Li1, Weier Bao1, Xiangxiang Kong1
1School of Chemical Sciences, University of Chinese Academy of Sciences (UCAS), Beijing 100049, P. R. China.
ACS applied bio materials
|January 29, 2026
概括
一种新的纳米剂,mSU@A-NPs@F-R,利用基 (•Cl) 和氧化 (NO) 的协同作用来增强抗瘤疗法. 这种纳米剂在 in vitro 和 in vivo 两种情况下都在破坏癌细胞方面表现出显著的有效性.
科学领域:
- 生物医学工程 生物医学工程
- 纳米技术纳米技术
- 癌症治疗 癌症治疗
背景情况:
- 基 (•Cl) 显示出在抗瘤治疗中增强氧化应激的潜力.
- 开发新的纳米剂对于协同的癌症治疗策略至关重要.
研究的目的:
- 开发一种核心纳米剂 (mSU@A-NPs@F-R) 用于癌症治疗.
- 为了利用光生成的基 (•Cl) 和氧化 (NO) 的协同作用.
主要方法:
- 使用上转化纳米粒子 (UCNP),AgCl纳米粒子和l-arginine制造mSU@A-NPs@F-R纳米剂.
- 通过近红外 (NIR) 光进行光激活,生成Cl和Ag原子.
- Ag原子调解了从l-氨酸中释放的NO,而NO增强了Cl生成.
主要成果:
- 在NIR光照射下,纳米剂有效地产生了Cl和NO.
- •Cl会诱导DNA和线粒体的氧化损伤.
- NO稳定了DNA损伤,并加剧了线粒体损伤,导致协同作用的癌细胞破坏.
- 在体外和体内活体瘤模型中证明了高疗效.
结论:
- 开发的mSU@A-NPs@F-R纳米剂为协同癌症治疗提供了一个有前途的战略.
- •Cl和NO的联合作用提供了增强的抗瘤作用.
- 这种方法有可能在未来的癌症治疗中进行临床转化.
相关概念视频
Oxidation Numbers
42.6K
In redox reactions, the transfer of electrons occurs between reacting species. Electron transfer is described by a hypothetical number called the oxidation number (or oxidation state). It represents the effective charge of an atom or element, which is assigned using a set of rules.
42.6K
Nitric Oxide Signaling Pathway
6.3K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
6.3K
Oxidation-Reduction Reactions
75.6K
Oxidation–Reduction Reactions
75.6K
Pyruvate Oxidation
168.8K
After glycolysis, the charged pyruvate molecules enter the mitochondria via active transport and undergo three enzymatic reactions. These reactions ensure that pyruvate can enter the next metabolic pathway so that energy stored in the pyruvate molecules can be harnessed by the cells.
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
168.8K
Radical Oxidation of Allylic and Benzylic Alcohols
2.9K
Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
2.9K
Radical Substitution: Allylic Chlorination
3.2K
Typically, when alkenes react with halogens at low temperatures, an addition reaction occurs. However, upon increasing the temperature or under reaction conditions that form radicals, providing a low but steady concentration of halogen radicals, allylic substitution reaction is favored. This is because allylic hydrogens are very reactive as the formed intermediate is resonance stabilized. For example, when propene is treated with chlorine in the gas phase at 400 °C, it undergoes allylic...
3.2K


