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Editorial

Pharmaceutical Biotechnology

by
Cesar Augusto Roque-Borda
*,
Fernando Rogério Pavan
* and
Andréía Bagliotti Meneguin
*
School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara 14800-903, SP, Brazil
*
Authors to whom correspondence should be addressed.
Life 2022, 12(8), 1240; https://doi.org/10.3390/life12081240
Submission received: 4 August 2022 / Accepted: 15 August 2022 / Published: 16 August 2022
(This article belongs to the Special Issue Pharmaceutical Biotechnology)
Biotechnology and pharmacy have shown efficient results when combined to generate innovative technological products [1]. In recent years, the increase in infectious diseases has led to economic decline and a global crisis [2]. The COVID-19 pandemic produced by SARS-CoV-2, a type of coronavirus, has taken the lives of millions of people in the last two years [3]. During this waiting time, the treatments adopted for infected patients have been based on the administration of azithromycin, and the effects of the uncontrolled use of this medication will be seen in years to come [4].
Pharmaceutical biotechnology has made it possible to quickly obtain vaccines and new recombinant drugs or drugs derived from living organisms that have a broad spectrum or specific action and manage to prevent diseases [5]. However, when it comes to infectious diseases, obtaining new drugs approved by the FDA is difficult because the ratio between reports of new MDR strains and new drugs is significantly large [6]. Concerning Mycobacterium tuberculosis, the bacterium that claims the most lives in the world, the registration of drugs is scarce or virtually non-existent [7]. The last drug to be approved (in 2012) was bedaquiline, and the bacterium has already shown resistance to almost all the drugs on the market. The seriousness of this problem led to a bedaquiline–protomanid combination (synergistic effect) to be approved in 2019 [8]. Therefore, the urgency for obtaining new drugs, especially for MDR bacteria classified as “critical and high priority” by the WHO, should be highlighted [9].
Thus, we have launched this Special Edition of Life called Pharmaceutical Biotechnology, where we frame the use of biomacromolecules that are being studied in depth, such as antimicrobial peptides, lipids, metal complexes, proteins, and toxins. Some molecules such as N-palmitoylethanolamide-oxazoline, i.e., an endogenous lipid, are able to regulate homeostasis and are involved in the modulation of inflammation; consequently, this molecules were shown to reduce intestinal damage in an animal model, namely zebrafish larvae [10]. This is an animal model with a high impact because it enables the replacement or reduction in the use of experimental mice [11].
Moreover, nanotechnology has shown promising results in the administration of drugs and the improvement of their activity. In this Special Issue, Salem et al. [12] report a study on selenium nanoparticles obtained from orange peel waste. These authors studied their properties against multidrug-resistant (MDR) bacteria such as P. aeruginosa, MDR E. coli, K. pneumonia, S. aureus ATCC 29213, and MDR clinical isolates, as well as their potential against the formation of biofilm of S. aureus clinical isolates. It is worth noting that these nanoparticles were obtained through green and environmentally friendly procedures, which is crucial in these times of environmental crisis [13]. Furthermore, a controlled transport mechanism in liquid crystals reported by Santos et al. [14] demonstrates the ability to sublingually administer rifampicin, with dose control and excellent anti-Mycobacterium tuberculosis activity after seven days of treatment.
Another highlight of these nanoformulations is reported by Elsewedy et al. [15]. These authors developed a hydrogel based on tea tree oil nanoemulsions for the purpose of improving the topical administration of neomycin, a drug used for bacterial skin infections. They demonstrate that the formulation was stable for up to three months and that there was no evidence of skin irritation. Likewise, Di Filippo et al. [16] report the development of microparticles formulated on the basis of chitosan loaded with ascorbic acid and nicotinamide, showing good physicochemical stability and dose-regulated protective antimicrobial activity. The authors demonstrated that there was no ex vivo permeation of the pig ear, which is excellent for the development of cosmetic formulations for the skin.
In summary, these results allow us to appreciate the great opportunities that the use of nanotechnology offers in the fight against MDR bacteria, improving the stability and administration of drugs against diseases or metabolic deregulations [5].

Funding

This editorial research was supported by São Paulo Research Foundation/FAPESP (process number #2016/00446-7; #2020/13497-4, #2018/25707-3 and #2020/16573-3).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The editors and collaborators of this Special Edition thank the researchers who contributed their articles for this section, allowing us to learn more about their scientific advances.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Roque-Borda, C.A.; da Silva, P.B.; Rodrigues, M.C.; Di Filippo, L.D.; Duarte, J.L.; Chorilli, M.; Vicente, E.F.; Garrido, S.S.; Pavan, F.R. Pharmaceutical Nanotechnology: Antimicrobial Peptides as potential new drugs against WHO list of critical, high, and medium priority bacteria. Eur. J. Med. Chem. 2022, 241, 114640. [Google Scholar] [CrossRef]
  2. Magana, M.; Pushpanathan, M.; Santos, A.L.; Leanse, L.; Fernandez, M.; Ioannidis, A.; Giulianotti, M.A.; Apidianakis, Y.; Bradfute, S.; Ferguson, A.L.; et al. The value of antimicrobial peptides in the age of resistance. Lancet Infect. Dis. 2020, 20, e216–e230. [Google Scholar] [CrossRef]
  3. Pai, M.; Kasaeva, T.; Swaminathan, S. COVID-19′s Devastating Effect on Tuberculosis Care—A Path to Recovery. N. Engl. J. Med. 2022, 386, 1490–1493. [Google Scholar] [CrossRef] [PubMed]
  4. Ghosh, S.; Bornman, C.; Zafer, M.M. Antimicrobial Resistance Threats in the emerging COVID-19 pandemic: Where do we stand? J. Infect. Public Health 2021, 14, 555–560. [Google Scholar] [CrossRef] [PubMed]
  5. Roque-Borda, C.A.; Gualque, M.W.d.L.; da Fonseca, F.H.; Pavan, F.R.; Santos-Filho, N.A. Nanobiotechnology with Therapeutically Relevant Macromolecules from Animal Venoms: Venoms, Toxins, and Antimicrobial Peptides. Pharmaceutics 2022, 14, 891. [Google Scholar] [CrossRef] [PubMed]
  6. Andrei, S.; Droc, G.; Stefan, G. FDA approved antibacterial drugs: 2018–2019. Discoveries 2019, 7, e102. [Google Scholar] [CrossRef] [PubMed]
  7. FDA. FDA Approves New Drug for Treatment-Resistant Forms of Tuberculosis That Affects the Lungs. Available online: https://www.fda.gov/news-events/press-announcements/fda-approves-new-drug-treatment-resistant-forms-tuberculosis-affects-lungs (accessed on 20 December 2021).
  8. Hoagland, D.T.; Liu, J.; Lee, R.B.; Lee, R.E. New agents for the treatment of drug-resistant Mycobacterium tuberculosis. Adv. Drug Deliv. Rev. 2016, 102, 55–72. [Google Scholar] [CrossRef] [PubMed]
  9. Roque-Borda, C.A.; da Silva, P.B.; Rodrigues, M.C.; Azevedo, R.B.; Di Filippo, L.; Duarte, J.L.; Chorilli, M.; Festozo Vicente, E.; Pavan, F.R. Challenge in the Discovery of New Drugs: Antimicrobial Peptides against WHO-List of Critical and High-Priority Bacteria. Pharmaceutics 2021, 13, 773. [Google Scholar] [CrossRef] [PubMed]
  10. Hasterok, R.; Betekhtin, A. Plant Cell and Organism Development 2.0. Int. J. Mol. Sci. 2022, 23, 1885. [Google Scholar] [CrossRef] [PubMed]
  11. Lu, J.-W.; Ho, Y.-J.; Ciou, S.-C.; Gong, Z. Innovative Disease Model: Zebrafish as an In Vivo Platform for Intestinal Disorder and Tumors. Biomedicines 2017, 5, 58. [Google Scholar] [CrossRef] [PubMed]
  12. Salem, S.S.; Badawy, M.S.E.M.; Al-Askar, A.A.; Arishi, A.A.; Elkady, F.M.; Hashem, A.H. Green Biosynthesis of Selenium Nanoparticles Using Orange Peel Waste: Characterization, Antibacterial and Antibiofilm Activities against Multidrug-Resistant Bacteria. Life 2022, 12, 893. [Google Scholar] [CrossRef]
  13. Lorenz, C.; Lage, M.d.O.; Chiaravalloti-Neto, F. Deforestation hotspots, climate crisis, and the perfect scenario for the next epidemic: The Amazon time bomb. Sci. Total Environ. 2021, 783, 147090. [Google Scholar] [CrossRef] [PubMed]
  14. Santos, K.P.; Rodero, C.F.; Ribeiro, C.M.; Gremião, M.P.D.; Peccinini, R.G.; Pavan, F.R.; Pearce, C.; Gonzalez-Juarrero, M.; Chorilli, M. Development of a Mucoadhesive Liquid Crystal System for the Administration of Rifampicin Applicable in Tuberculosis Therapy. Life 2022, 12, 1138. [Google Scholar] [CrossRef]
  15. Elsewedy, H.S.; Shehata, T.M.; Soliman, W.E. Tea Tree Oil Nanoemulsion-Based Hydrogel Vehicle for Enhancing Topical Delivery of Neomycin. Life 2022, 12, 1011. [Google Scholar] [CrossRef] [PubMed]
  16. Di Filippo, L.D.; Duarte, J.L.; Roque-Borda, C.A.; Pavan, F.R.; Meneguin, A.B.; Chorilli, M.; Melero, A.; Guillot, A.J.; Spagnol, C.M.; Correa, M.A. In Vitro Skin Co-Delivery and Antibacterial Properties of Chitosan-Based Microparticles Containing Ascorbic Acid and Nicotinamide. Life 2022, 12, 1049. [Google Scholar] [CrossRef] [PubMed]
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MDPI and ACS Style

Roque-Borda, C.A.; Pavan, F.R.; Meneguin, A.B. Pharmaceutical Biotechnology. Life 2022, 12, 1240. https://doi.org/10.3390/life12081240

AMA Style

Roque-Borda CA, Pavan FR, Meneguin AB. Pharmaceutical Biotechnology. Life. 2022; 12(8):1240. https://doi.org/10.3390/life12081240

Chicago/Turabian Style

Roque-Borda, Cesar Augusto, Fernando Rogério Pavan, and Andréía Bagliotti Meneguin. 2022. "Pharmaceutical Biotechnology" Life 12, no. 8: 1240. https://doi.org/10.3390/life12081240

APA Style

Roque-Borda, C. A., Pavan, F. R., & Meneguin, A. B. (2022). Pharmaceutical Biotechnology. Life, 12(8), 1240. https://doi.org/10.3390/life12081240

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