Synthesis of PEGylation hydroxyapatite drug delivery system and its dual channels fluorescence imaging

Xiaojing LI; Wen SUN; Yao KANG; Jiangli FAN; Xiaojun PENG

doi:10.11949/0438-1157.20200780

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Synthesis of PEGylation hydroxyapatite drug delivery system and its dual channels fluorescence imaging

Material science and engineering, nanotechnology | 更新时间：2025-11-25

- Synthesis of PEGylation hydroxyapatite drug delivery system and its dual channels fluorescence imaging
- CIESC Journal Vol. 71, Issue 10, Pages: 4808-4819(2020)
- 作者机构：
  
  大连理工大学精细化工国家重点实验室，辽宁大连 116024
- 作者简介：
- 基金信息：
- DOI：10.11949/0438-1157.20200780
  CLC： TQ 34
- Received：19 June 2020，
  
  Revised：2020-07-23，
  
  Published：05 October 2020
- 稿件说明：
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李晓静, 孙文, 康垚, 樊江莉, 彭孝军. PEG化羟基磷灰石纳米体系的制备及双通道荧光成像[J]. 化工学报, 2020, 71(10): 4808-4819

LI Xiaojing, SUN Wen, KANG Yao, FAN Jiangli, PENG Xiaojun. Synthesis of PEGylation hydroxyapatite drug delivery system and its dual channels fluorescence imaging[J]. CIESC Journal, 2020, 71(10): 4808-4819
李晓静, 孙文, 康垚, 樊江莉, 彭孝军. PEG化羟基磷灰石纳米体系的制备及双通道荧光成像[J]. 化工学报, 2020, 71(10): 4808-4819 DOI： 10.11949/0438-1157.20200780.

LI Xiaojing, SUN Wen, KANG Yao, FAN Jiangli, PENG Xiaojun. Synthesis of PEGylation hydroxyapatite drug delivery system and its dual channels fluorescence imaging[J]. CIESC Journal, 2020, 71(10): 4808-4819 DOI： 10.11949/0438-1157.20200780.

摘要

PEG化的药物递送系统（DDSs）可以通过增强药物的渗透性和滞留性（EPR）效应克服传统化疗的副作用。利用共沉淀法和水热法制备纳米粒子DOX@HAP，进一步通过偶联反应修饰菁染料（Cy），通过铜（I）催化的炔-叠氮化物环加成反应修饰PEG链，构建了纳米制剂DOX@HAP-Cy-PEG。通过透射电子显微镜（TEM）、扫描电子显微镜（SEM）、粒度分析仪、傅里叶红外光谱仪（FTIR）、X射线光电子能谱仪（XPS）和X射线衍射仪（XRD）对该纳米载药体系的形貌、粒径、物相组成进行表征分析。利用紫外-可见（UV-Vis）分光光度法测定了该纳米材料的药物负载量以及体外药物释放曲线。进一步，利用DOX和Cy双通道荧光成像，监测DDSs在Hela和HepG2细胞中的摄取行为。表明DOX@HAP-Cy-PEG纳米载药体系有望作为一种新型的治疗与示踪一体化的抗癌纳米制剂。

Abstract

PEGylated drug delivery systems (DDSs) can overcome the side effects of traditional chemotherapy by enhancing drug permeability and retention (EPR) effects. In this work

DOX@HAP (hydroxyapatite) was initially fabricated

via

the coprecipitation and hydrothermal method

further functionalized with Cy (cyanine) by coupling reaction of APTES and then introduced hydrophilic PEG chains by using copper(I)-catalyzed alkyne–azide cycloaddition reaction. Physicochemical properties including the morphology

particle size and phase composition

were characterized by TEM

SEM

particle size analyzer

FTIR

XPS and XRD. The encapsulation efficiency and drug release profile of DOX@HAP-Cy-PEG were analyzed by UV-Vis spectrophotometry. Furthermore

the cellular uptake of DOX@HAP-Cy-PEG nanoparticles in Hela and HepG2 cells was monitored by the dual channels fluorescence imaging of DOX and Cy. The results showed that DOX@HAP-Cy-PEG nanoparticles could be used to real-time monitor the dynamic distribution of DDSs in Hela and HepG2 cells by dual channels.

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references

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