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Effect of different silica coatings on the toxicity of upconversion nanoparticles on RAW 264.7 macrophage cells

机译:不同二氧化硅涂层对原料264.7巨噬细胞上转化纳米粒子毒性的影响

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摘要

Upconversion nanoparticles (UCNPs), consisting of NaYF4 doped with 18% Yb and 2% Er, were coated with microporous silica shells with thickness values of 7 ± 2 and 21 ± 3 nm. Subsequently, the negatively charged particles were functionalized with N-(6-aminohexyl)-3-aminopropyltrimethoxysilane (AHAPS), which provide a positive charge to the nanoparticle surface. Inductively coupled plasma optical emission spectrometry (ICP-OES) measurements revealed that, over the course of 24h, particles with thicker shells release fewer lanthanide ions than particles with thinner shells. However, even a 21 ± 3 nm thick silica layer does not entirely block the disintegration process of the UCNPs. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays and cell cytometry measurements performed on macrophages (RAW 264.7 cells) indicate that cells treated with amino-functionalized particles with a thicker silica shell have a higher viability than those incubated with UCNPs with a thinner silica shell, even if more particles with a thicker shell are taken up. This effect is less significant for negatively charged particles. Cell cycle analyses with amino-functionalized particles also confirm that thicker silica shells reduce cytotoxicity. Thus, growing silica shells to a sufficient thickness is a simple approach to minimize the cytotoxicity of UCNPs.
机译:由掺杂有18%Yb和2%ER的Nayf4的上转化纳米颗粒(UCNP)组成,用微孔二氧化硅壳涂覆,厚度值为7±2和21±3nm。随后,用N-(6-氨基己基)-3-氨基丙基三甲氧基硅烷(凹槽)官能化的带负电荷的颗粒,其为纳米颗粒表面提供正电荷。电感耦合等离子体光发射光谱法(ICP-OES)测量显示,在24h的过程中,含有较厚壳的颗粒释放较少的镧系元素,较薄的壳。然而,即使是21±3nm厚的二氧化硅层也不完全阻断UCNP的崩解过程。在巨噬细胞(RAW 264.7细胞)上进行的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴铵(MTT)测定和细胞细胞计量测量结果表明用氨基官能化颗粒用较厚的二氧化硅壳处理的细胞具有比用较薄的二氧化硅壳温育的可活力,即使吸收更厚的壳的颗粒也是如此。这种效果对带负电荷的颗粒不太重要。用氨基官能化颗粒分析细胞周期分析还证实较厚的二氧化硅壳减少了细胞毒性。因此,将硅壳生长至足够的厚度是最小化UCNP的细胞毒性的简单方法。

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