Rudra Narayan Subudhi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Rudra Narayan Subudhi has a total of 25 co-authors. Here are the top co-authors by number of shared publications:
- Manoj Dalabehera
Uttaranchal University
4 shared publications - Shubham Chaudhari
Institute of Pharmaceutical Sciences, J.S. University, Shikohabad, India, J.S. Universityin, Shikohabad, India
3 shared publications - Alka Kumari
University Institute of Pharma Sciences, Chandigarh University, Ajitgarh, Punjab, India, Chandigarh University, Mohali-140413, India
2 shared publications - Charul Rathore
University Institute of Pharma Sciences, Chandigarh University, Ajitgarh, Punjab, India, Chandigarh University, Mohali-140413, India
2 shared publications - Abdulrahman Mohammed Alhudhaibi
Department of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia
1 shared publication Ana Figueiras
Laboratory of Drug Development and Technologies, Faculty of Pharmacy, University of Coimbra,3000-548 Coimbra, Portugal; REQUIMTE/LAQV, Group of Pharmaceutical Technology, University of Coimbra, 3000-548 Coimbra, Portugal
1 shared publication
Latest Publications
- 28 July 2026
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 115 (9) , 104442
Mechanistic advances in nanomedicine, nucleic acid therapies, and AI-driven research on cervical cancer
- 28 July 2026
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 115 (9) , 104442
Mechanistic advances in nanomedicine, nucleic acid therapies, and AI-driven research on cervical cancer
- Open Access
- 21 November 2025
- Published by Elsevier in Materials Today Bio
- Vol. 35
mRNA delivery systems 2.0: Engineering extrahepatic delivery for non-vaccine therapeutics
- 21 November 2025
- Published by Elsevier in Materials Today Bio
- Vol. 35
Open AccessmRNA delivery systems 2.0: Engineering extrahepatic delivery for non-vaccine therapeutics
- 22 October 2025
- Published by Springer Nature in Journal of Pharmaceutical Innovation
- Vol. 20 (6) , 1-20
Fabrication and Optimization of Chebulinic Acid-Loaded Liposomes Based on Carbopol-gel Employing Box-Behnken Design for Vulvovaginal Candidiasis
- 22 October 2025
- Published by Springer Nature in Journal of Pharmaceutical Innovation
- Vol. 20 (6) , 1-20
Fabrication and Optimization of Chebulinic Acid-Loaded Liposomes Based on Carbopol-gel Employing Box-Behnken Design for Vulvovaginal Candidiasis
- Open Access
- 21 October 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (10) , 2411
Natural Molecules, Nutraceuticals, and Engineered Nanosystems: A Comprehensive Strategy for Combating Gardnerella vaginalis-Induced Bacterial Vaginosis
Bacterial vaginosis (BV) is a highly prevalent vaginal infection characterized by a dysbiotic shift in the vaginal microbiota, with Gardnerella vaginalis acting as a principal pathogen. Despite its association with adverse reproductive outcomes, BV remains underexplored from both mechanistic and therapeutic standpoints. Standard antibiotic regimens frequently fail due to high recurrence rates driven by multidrug-resistant (MDR) G. vaginalis strains and biofilm formation. In response, natural compounds and nutraceuticals, owing to their intrinsic antibacterial, antibiofilm, and immunomodulatory properties, have emerged as promising candidates for alternative BV therapies. In this paper, we first compile and critically evaluate preclinical and clinical evidence on the efficacy of plant extracts, essential oils (EOs), probiotics, vitamins, proteins, fatty acids, and enzymes against G. vaginalis, emphasizing their mechanistic insights in restoring vaginal microbial balance. Next, we focus on the integration of these bioactive agents into engineered nanosystems, such as lipid-based nanoparticles (LNPs), polymeric carriers, and inorganic nanostructures, to overcome limitations related to solubility, stability, and targeted delivery. Nonetheless, comparative studies, combination therapies, and recent patent developments are discussed to highlight how naturally derived molecules can enhance antimicrobial potency and reduce cytotoxicity. In conclusion, these platforms demonstrate superior in vitro and in vivo efficacy, offering a paradigm shift in the management of BV. Key challenges include scalable manufacturing, regulatory approval, and comprehensive safety assessment. Future research should prioritize standardized nanoparticle (NP) synthesis, detailed pharmacokinetic and toxicity profiling, and well-designed clinical trials to validate nature-inspired, nanoengineered therapies against G. vaginalis-induced BV.
- 21 October 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (10) , 2411
Open AccessNatural Molecules, Nutraceuticals, and Engineered Nanosystems: A Comprehensive Strategy for Combating Gardnerella vaginalis-Induced Bacterial Vaginosis
Bacterial vaginosis (BV) is a highly prevalent vaginal infection characterized by a dysbiotic shift in the vaginal microbiota, with Gardnerella vaginalis acting as a principal pathogen. Despite its association with adverse reproductive outcomes, BV remains underexplored from both mechanistic and therapeutic standpoints. Standard antibiotic regimens frequently fail due to high recurrence rates driven by multidrug-resistant (MDR) G. vaginalis strains and biofilm formation. In response, natural compounds and nutraceuticals, owing to their intrinsic antibacterial, antibiofilm, and immunomodulatory properties, have emerged as promising candidates for alternative BV therapies. In this paper, we first compile and critically evaluate preclinical and clinical evidence on the efficacy of plant extracts, essential oils (EOs), probiotics, vitamins, proteins, fatty acids, and enzymes against G. vaginalis, emphasizing their mechanistic insights in restoring vaginal microbial balance. Next, we focus on the integration of these bioactive agents into engineered nanosystems, such as lipid-based nanoparticles (LNPs), polymeric carriers, and inorganic nanostructures, to overcome limitations related to solubility, stability, and targeted delivery. Nonetheless, comparative studies, combination therapies, and recent patent developments are discussed to highlight how naturally derived molecules can enhance antimicrobial potency and reduce cytotoxicity. In conclusion, these platforms demonstrate superior in vitro and in vivo efficacy, offering a paradigm shift in the management of BV. Key challenges include scalable manufacturing, regulatory approval, and comprehensive safety assessment. Future research should prioritize standardized nanoparticle (NP) synthesis, detailed pharmacokinetic and toxicity profiling, and well-designed clinical trials to validate nature-inspired, nanoengineered therapies against G. vaginalis-induced BV.