Aptamer-Conjugated Multi-Quantum Dot-Embedded Silica Nanoparticles for Lateral Flow Immunoassay

Author:

Yoo Kwanghee1ORCID,Cho Hye-Seong1,Kim Jaehi1,Shin Minsup1,Chu Jun-Sik1,Jang Sohyeon1,Bae Han-Joo1,Jung Heung Su2ORCID,Kang Homan3ORCID,Jun Bong-Hyun1ORCID

Affiliation:

1. Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Republic of Korea

2. Company of Global Zeus, Hwaseong 18363, Republic of Korea

3. Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA

Abstract

Lateral flow immunoassays (LFIAs) are widely used for their low cost, simplicity, and rapid results; however, enhancing their reliability requires the meticulous selection of ligands and nanoparticles (NPs). SiO2@QD@SiO2 (QD2) nanoparticles, which consist of quantum dots (QDs) embedded in a silica (SiO2) core and surrounded by an outer SiO2 shell, exhibit significantly higher fluorescence intensity (FI) compared to single QDs. In this study, we prepared QD2@PEG@Aptamer, an aptamer conjugated with QD2 using succinimidyl-[(N-maleimidopropionamido)-hexaethyleneglycol]ester, which is 130 times brighter than single QDs, for detecting carbohydrate antigen (CA) 19-9 through LFIA. For LFIA optimization, we determined the optimal conditions as a 1.0:2.0 × 10−2 ratio of polyethylene glycol (PEG) to aptamer by adjusting the amounts of PEG and aptamer, phosphate-buffered saline containing 0.5% Tween® 20 as a developing solution, and 0.15 μg NPs by setting the NP weight during development. Under these conditions, QD2@PEG@Aptamer selectively detected CA19-9, achieving a detection limit of 1.74 × 10−2 mg·mL−1. Moreover, FI remained stable for 10 days after detection. These results highlight the potential of QD2 and aptamer conjugation technology as a reliable and versatile sensing platform for various diagnostic applications.

Funder

Konkuk University

Publisher

MDPI AG

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