Apoferritin and Dps as drug delivery vehicles: Some selected examples in oncology.

Apoferritin Cancer DNA binding proteins from starved cells Drug targeting Nanoparticles Oncology Therapeutics

Journal

Biochimica et biophysica acta. General subjects
ISSN: 1872-8006
Titre abrégé: Biochim Biophys Acta Gen Subj
Pays: Netherlands
ID NLM: 101731726

Informations de publication

Date de publication:
02 2022
Historique:
received: 23 06 2021
revised: 27 11 2021
accepted: 02 12 2021
pubmed: 14 12 2021
medline: 17 2 2022
entrez: 13 12 2021
Statut: ppublish

Résumé

The ideal nanoparticle should be able to encapsulate either pharmaceutical agents or imaging probes so that it could treat or image clinical tumours by targeting the cancer site efficiently. Further, it would be an added advantage if it demonstrates: small size, built in targeting, biocompatibility and biodegradability. Ferritin, which is an endogenous self-assembling protein, stores iron and plays a role in iron homeostasis. When iron atoms are removed apoferritin (AFt) is formed which consists of a hollow shell where it can be used to load guest molecules. Due to its unique architecture, AFt has been investigated as a versatile carrier for tumour theranostic applications. DNA-binding protein from starved cells (Dps), which also belongs to the ferritin family, is a protein found only in prokaryotes. It is used to store iron and protect chromosomes from oxidative damage; because of its architecture, Dps could also be used as a delivery vehicle. Both these nano particles are promising in the field of oncology, especially due to their stability, solubility and biocompatibility features. Further their exterior surface can be modified for better tumour-targeting ability. More studies, are warranted to determine the immunogenicity, biodistribution, and clearance from the body. This review discusses a few selected examples of the remarkable in vitro and in vivo studies that have been carried out in the recent past with the use of AFt and Dps in targeting and delivery of various pharmaceutical agents, natural products and imaging probes in the field of oncology.

Sections du résumé

BACKGROUND
The ideal nanoparticle should be able to encapsulate either pharmaceutical agents or imaging probes so that it could treat or image clinical tumours by targeting the cancer site efficiently. Further, it would be an added advantage if it demonstrates: small size, built in targeting, biocompatibility and biodegradability. Ferritin, which is an endogenous self-assembling protein, stores iron and plays a role in iron homeostasis. When iron atoms are removed apoferritin (AFt) is formed which consists of a hollow shell where it can be used to load guest molecules. Due to its unique architecture, AFt has been investigated as a versatile carrier for tumour theranostic applications. DNA-binding protein from starved cells (Dps), which also belongs to the ferritin family, is a protein found only in prokaryotes. It is used to store iron and protect chromosomes from oxidative damage; because of its architecture, Dps could also be used as a delivery vehicle.
CONCLUSIONS
Both these nano particles are promising in the field of oncology, especially due to their stability, solubility and biocompatibility features. Further their exterior surface can be modified for better tumour-targeting ability. More studies, are warranted to determine the immunogenicity, biodistribution, and clearance from the body.
GENERAL PERSPECTIVE
This review discusses a few selected examples of the remarkable in vitro and in vivo studies that have been carried out in the recent past with the use of AFt and Dps in targeting and delivery of various pharmaceutical agents, natural products and imaging probes in the field of oncology.

Identifiants

pubmed: 34896255
pii: S0304-4165(21)00226-9
doi: 10.1016/j.bbagen.2021.130067
pii:
doi:

Substances chimiques

Apoferritins 9013-31-4

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

130067

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Anchala I Kuruppu (AI)

Institute for Combinatorial Advanced Research & Education, General Sir John Kotelawala Defence University, Sri Lanka. Electronic address: kuruppua@kdu.ac.lk.

Lyudmila Turyanska (L)

Faculty of Engineering, University of Nottingham, UK.

Tracey D Bradshaw (TD)

School of Pharmacy, University of Nottingham, UK.

Sivakumar Manickam (S)

Petroleum and Chemical Engineering, Faculty of Engineering, Universiti Teknologi Brunei, Brunei Darussalam.

Bandula Prasanna Galhena (BP)

Department Biochemistry and Clinical Chemistry, Faculty of Medicine, University of Kelaniya, Sri Lanka.

Priyani Paranagama (P)

Department of Chemistry, Faculty of Science, University of Kelaniya, Sri Lanka; Institute of Indigenous Medicine, University of Colombo, Sri Lanka.

Ranil De Silva (R)

Institute for Combinatorial Advanced Research & Education, General Sir John Kotelawala Defence University, Sri Lanka.

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Classifications MeSH