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AS1411 aptamer/RGD dual functionalized theranostic chitosan-PLGA nanoparticles for brain cancer treatment and imaging.
- Source :
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Biomaterials advances [Biomater Adv] 2024 Jun; Vol. 160, pp. 213833. Date of Electronic Publication: 2024 Mar 20. - Publication Year :
- 2024
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Abstract
- Conventional chemotherapy and poor targeted delivery in brain cancer resulting to poor treatment and develop resistance to anticancer drugs. Meanwhile, it is quite challenging to diagnose/detection of brain tumor at early stage of cancer which resulting in severity of the disease. Despite extensive research, effective treatment with real-time imaging still remains completely unavailable, yet. In this study, two brain cancer cell specific moieties i.e., AS1411 aptamer and RGD are decorated on the surface of chitosan-PLGA nanoparticles to improve targeted co-delivery of docetaxel (DTX) and upconversion nanoparticles (UCNP) for effective brain tumor therapy and real-time imaging. The nanoparticles were developed by a slightly modified emulsion/solvent evaporation method. This investigation also translates the successful synthesis of TPGS-chitosan, TPGS-RGD and TPGS-AS1411 aptamer conjugates for making PLGA nanoparticle as a potential tool of the targeted co-delivery of DTX and UCNP to the brain cancer cells. The developed nanoparticles have shown an average particle size <200 nm, spherical in shape, high encapsulation of DTX and UCNP in the core of nanoparticles, and sustained release of DTX up to 72 h in phosphate buffer saline (pH 7.4). AS1411 aptamer and RGD functionalized theranostic chitosan-PLGA nanoparticles containing DTX and UCNP (DUCPN-RGD-AS1411) have achieved greater cellular uptake, 89-fold improved cytotoxicity, enhanced cancer cell arrest even at lower drug conc., improved bioavailability with higher mean residence time of DTX in systemic circulation and brain tissues. Moreover, DUCPN-RGD-AS1411 have greatly facilitated cellular internalization and higher accumulation of UCNP in brain tissues. Additionally, DUCPN-RGD-AS1411 demonstrated a significant suppression in tumor growth in brain-tumor bearing xenograft BALB/c nude mice with no impressive sign of toxicities. DUCPN-RGD-AS1411 has great potential to be utilized as an effective and safe theranostic tool for brain cancer and other life-threatening cancer therapies.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Humans
Mice
Antineoplastic Agents administration & dosage
Antineoplastic Agents pharmacology
Antineoplastic Agents pharmacokinetics
Antineoplastic Agents therapeutic use
Antineoplastic Agents chemistry
Cell Line, Tumor
Nanoparticles chemistry
Oligopeptides chemistry
Oligopeptides administration & dosage
Oligopeptides pharmacokinetics
Theranostic Nanomedicine methods
Aptamers, Nucleotide administration & dosage
Aptamers, Nucleotide chemistry
Aptamers, Nucleotide pharmacokinetics
Brain Neoplasms drug therapy
Brain Neoplasms pathology
Brain Neoplasms diagnostic imaging
Brain Neoplasms metabolism
Chitosan chemistry
Docetaxel pharmacokinetics
Docetaxel administration & dosage
Docetaxel pharmacology
Docetaxel therapeutic use
Oligodeoxyribonucleotides
Polylactic Acid-Polyglycolic Acid Copolymer chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 2772-9508
- Volume :
- 160
- Database :
- MEDLINE
- Journal :
- Biomaterials advances
- Publication Type :
- Academic Journal
- Accession number :
- 38564997
- Full Text :
- https://doi.org/10.1016/j.bioadv.2024.213833