Prodrug-Based Nanodelivery Strategies

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmaceutical Technology".

Deadline for manuscript submissions: closed (30 November 2022) | Viewed by 5153

Special Issue Editor

Department of Pharmacy, Chia Nan University of Pharmacy and Science, Tainan 717, Taiwan
Interests: tumor-activated prodrugs; liposomes; nanomedicines

Special Issue Information

Dear Colleagues,

Chemotherapy is an important treatment modality for many cancers; however, its use is often palliative rather than curative. The basic limitation of chemotherapy is the physiological similarity between normal and tumor cells. Tumor-activated prodrugs have been proposed for drug targeting of tumor cells. The aim of prodrug establishment is to improve toxicity selectivity and physicochemical properties such as solubility and chemical stability. This strategy exploits unique aspects of tumor physiology such as selective enzyme expression or hypoxia. Hence, this strategy is limited to tumor conditions.

Nanodelivery systems represent a relatively new but rapidly developing science, and they are employed in the delivery of therapeutic agents to specific targeted sites in a controlled manner. Nanomaterials can be well defined as a material, with sizes ranging between 1 and 100 nm, which influences drug delivery to tissue engineering, such as in the case of liposomes. Liposomes are now FDA-approved and represent the first generation of nanoparticle-based therapy. Liposomes stay in the blood circulatory system for a prolonged period and enable the release of amalgamated drugs as per the specified dose. Thus, they cause fewer plasma fluctuations with reduced adverse effects. Being nano-sized, the liposomes penetrate the tissue system, facilitate easy uptake of the drug by cells, permit efficient drug delivery, and ensure action at the targeted location.

Encapsulation of prodrugs in liposomes makes them nanomedicines, which can be used in selective targeting of tumors due to the permeability and retention effect, a phenomenon in which nanoparticles can diffuse through relatively large pores in blood vessels and accumulate at tumor sites. Hence, prodrug-based nanodelivery is a prospective approach to increase the selectivity and efficacy of cancer therapy.

Dr. Yulin Leu
Guest Editor

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Keywords

  • tumor-activated prodrugs
  • glucuronide prodrug
  • antitumor agents
  • liposomes
  • nanomedicines

Published Papers (2 papers)

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Research

19 pages, 9190 KiB  
Article
A Novel Hydroxyapatite/Vitamin B12 Nanoformula for Treatment of Bone Damage: Preparation, Characterization, and Anti-Arthritic, Anti-Inflammatory, and Antioxidant Activities in Chemically Induced Arthritic Rats
by Amany Belal, Rehab Mahmoud, Eman E. Mohamed, Ahmed Farghali, Fatma I. Abo El-Ela, Amr Gamal, Fatma Mohamed Halfaya, Esraa Khaled, Abdelbasset A. Farahat, Ahmed H. E. Hassan, Mohammed M. Ghoneim, Mohamed Taha and Mohamed Y. Zaky
Pharmaceuticals 2023, 16(4), 551; https://doi.org/10.3390/ph16040551 - 6 Apr 2023
Cited by 4 | Viewed by 2320
Abstract
The usage of nanomaterials for rheumatoid arthritis (RA) treatment can improve bioavailability and enable selective targeting. The current study prepares and evaluates the in vivo biological effects of a novel hydroxyapatite/vitamin B12 nanoformula in Complete Freund’s adjuvant-induced arthritis in rats. The synthesized [...] Read more.
The usage of nanomaterials for rheumatoid arthritis (RA) treatment can improve bioavailability and enable selective targeting. The current study prepares and evaluates the in vivo biological effects of a novel hydroxyapatite/vitamin B12 nanoformula in Complete Freund’s adjuvant-induced arthritis in rats. The synthesized nanoformula was characterized using XRD, FTIR, BET analysis, HERTEM, SEM, particle size, and zeta potential. We synthesized pure HAP NPs with 71.01% loading weight percentages of Vit B12 and 49 mg/g loading capacity. Loading of vitamin B12 on hydroxyapatite was modeled by Monte Carlo simulation. Anti-arthritic, anti-inflammatory, and antioxidant effects of the prepared nanoformula were assessed. Treated arthritic rats showed lower levels of RF and CRP, IL-1β, TNF-α, IL-17, and ADAMTS-5, but higher IL-4 and TIMP-3 levels. In addition, the prepared nanoformula increased GSH content and GST antioxidant activity while decreasing LPO levels. Furthermore, it reduced the expression of TGF-β mRNA. Histopathological examinations revealed an improvement in joint injuries through the reduction of inflammatory cell infiltration, cartilage deterioration, and bone damage caused by Complete Freund’s adjuvant. These findings indicate that the anti-arthritic, antioxidant, and anti-inflammatory properties of the prepared nanoformula could be useful for the development of new anti-arthritic treatments. Full article
(This article belongs to the Special Issue Prodrug-Based Nanodelivery Strategies)
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21 pages, 6518 KiB  
Article
Therapeutic Potential of Zeolites/Vitamin B12 Nanocomposite on Complete Freund’s Adjuvant-Induced Arthritis as a Bone Disorder: In Vivo Study and Bio-Molecular Investigations
by Amany Belal, Rehab Mahmoud, Mohamed Taha, Fatma Mohamed Halfaya, Ahmed Hassaballa, Esraa Salah Elbanna, Esraa Khaled, Ahmed Farghali, Fatma I. Abo El-Ela, Samar M. Mahgoub, Mohammed M. Ghoneim and Mohamed Y. Zaky
Pharmaceuticals 2023, 16(2), 285; https://doi.org/10.3390/ph16020285 - 13 Feb 2023
Cited by 2 | Viewed by 2447
Abstract
Rheumatoid arthritis (RA) is a long-term autoimmune disease. As nanotechnology has advanced, a growing number of nanodrugs have been used in the treatment of RA due to their unique physical and chemical properties. The purpose of this study was to assess the therapeutic [...] Read more.
Rheumatoid arthritis (RA) is a long-term autoimmune disease. As nanotechnology has advanced, a growing number of nanodrugs have been used in the treatment of RA due to their unique physical and chemical properties. The purpose of this study was to assess the therapeutic potential of a novel zeolite/vitamin B12 nanocomposite (Nano ZT/Vit B12) formulation in complete Freund’s adjuvant (CFA)-induced arthritis. The newly synthesized Nano ZT/Vit B12 was fully characterized using various techniques such as XRD, FT-IR, BET analysis, HERTEM, SEM, practical size, zeta potential, XRF, and EDX. The anti-arthritic, anti-inflammatory, and antioxidant activities as well as the immunomodulation effect of Nano ZT/Vit B12 on the CFA rat model of arthritis were examined. Histopathologic ankle joint injuries caused by CFA intrapedal injection included synovium hyperplasia, inflammatory cell infiltration, and extensive cartilage deterioration. The arthritic rats’ Nano ZT/Vit B12 supplementation significantly improved these effects. Furthermore, in arthritic rats, Nano ZT/Vit B12 significantly reduced serum levels of RF and CRP, as well as the levels of IL-1β, TNF-α, IL-17, and ADAMTS-5, while increasing IL-4 and TIMP-3 levels. Nano-ZT/Vit B12 significantly declined the LPO level and increased antioxidant activities, such as GSH content and GST activity, in the arthritic rats. In arthritic rats, Nano ZT/Vit B12 also reduced TGF-β mRNA gene expression and MMP-13 protein levels. Collectively, Nano ZT/Vit B12 seems to have anti-arthritic, anti-inflammatory, and antioxidant properties, making it a promising option for RA in the future. Full article
(This article belongs to the Special Issue Prodrug-Based Nanodelivery Strategies)
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