Diah Ratnadewi

Dr. Diah Ratnadewi

Professor in Biology Department-IPB University

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 August 2004 in Planta
Verified
Journal Article
Closed access
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WFWolfgang Frank
Wolfgang Frank
DRDiah Ratnadewi
Diah Ratnadewi
RRRalf Reski
Ralf Reski

29 March 2023 in Biomedicines
Verified
Journal Article
Open access
PDF file
ASAndari Sarasati
Andari Sarasati
Muhammad Hidayat SyahruddinMuhammad Hidayat Syahruddin
Muhammad Hidayat Syahruddin
ANArchadian Nuryanti
Archadian Nuryanti
IAIka Dewi Ana
Ika Dewi Ana
ABAnggraini Barlian
Anggraini Barlian
HTHiroshi Takemori
Hiroshi Takemori
Plant-derived exosome-like nanoparticles (PDENs) comprise various bioactive biomolecules. As an alternative cell-free therapeutic approach, they have the potential to deliver nano-bioactive compounds to the human body, and thus lead to various anti-inflammatory, antioxidant, and anti-tumor benefits. Moreover, it is known that Indonesia is one of the herbal centers of the world, with an abundance of unexplored sources of PDENs. This encouraged further research in biomedical science to develop natural richness in plants as a source for human welfare. This study aims to verify the potential of PDENs for biomedical purposes, especially for regenerative therapy applications, by collecting and analyzing data from the latest relevant research and developments.

7 August 2007 in The Plant Journal
Verified
Journal Article
Closed access
PDF file
WFWolfgang Frank
Wolfgang Frank
KBKim‐Miriam Baar
Kim‐Miriam Baar
EQEnas Qudeimat
Enas Qudeimat
MWMayada Woriedh
Mayada Woriedh
AAAli Alawady
Ali Alawady
RRRalf Reski
Ralf Reski

8 January 2021 in Metabolites
Verified
Journal Article
Open access
PDF file
Abdul Halim UmarAbdul Halim Umar
Abdul Halim Umar
DRDiah Ratnadewi
Diah Ratnadewi
Mohamad RafiMohamad Rafi
Mohamad Rafi
YSYohana Caecilia Sulistyaningsih
Yohana Caecilia Sulistyaningsih
Curculigo orchioides and C. latifolia have been used as traditional medicines such as antidiabetic and anticancer. This study measured the total phenolics and flavonoid contents as well as analyzed the functional groups and chemical compounds using Fourier-transform infrared (FTIR) spectra and UHPLC-Q-Orbitrap-HRMS profiling for the discrimination of plant parts, geographical origin, and compounds that presumably have a significant contribution as antioxidant and α-glucosidase inhibitors on both plants. The total phenolics and flavonoids contents in Curculigo species varied from 142.09 to 452.47 mg gallic acid equivalent (GAE/g) and from 0.82 to 5.44 mg quercetin equivalent (QE/g), respectively. The lowest IC50 for antioxidant and α-glucosidase inhibitory activities is presented by C. latifolia from a higher altitude region. Principal component analysis (PCA) from FTIR and UHPLC-Q-Orbitrap-HRMS data could discriminate the plant parts and geographical origin. Partial least squares (PLS) analysis has identified several functional groups, such as O–H, C–H, C=O, C–C, C–O, and chemical compounds, unknown-185 and unknown-85, that are most likely to contribute to the antioxidant and α-glucosidase inhibitory activities.

1 June 2012 in HAYATI Journal of Biosciences
Verified
Journal Article
Open access
PDF file
SUSumaryono
Sumaryono
WMWirdhatul Muslihatin
Wirdhatul Muslihatin
DRDiah Ratnadewi
Diah Ratnadewi
Effect of Carbohydrate Source on Growth and Performance of In Vitro Sago Palm (Metroxylon sagu Rottb.) Plantlets

27 October 2022 in Journal of Biomolecular Structure and Dynamics
Verified
Journal Article
Closed access
Abdul Halim UmarAbdul Halim Umar
Abdul Halim Umar
DRDiah Ratnadewi
Diah Ratnadewi
Mohamad RafiMohamad Rafi
Mohamad Rafi
YSYohana Caecilia Sulistyaningsih
Yohana Caecilia Sulistyaningsih
HHHamim Hamim
Hamim Hamim
WKWisnu Ananta Kusuma
Wisnu Ananta Kusuma
Curculigo spp. is a herb that is commonly used in Indonesia to treat diabetes mellitus (DM) . The main active components of Curculigo spp. were identified through our previous metabolomic study and online database platform. However, the biological mechanisms underlying Curculigo spp. activity in treating DM remain unclear. Therefore, in this study, a network pharmacology was used to explore the active compounds of Curculigo spp. and their potential molecular mechanisms for treating DM. Oral bioavailability and drug-likeness from the compounds of Curculigo spp. were screened using Lipinski’s rule of five, BBB, HIA + and Caco-2 permeability criteria. A network of compound–target–disease–pathway was then constructed using Cytoscape. The highest degree compounds and targets were then confirmed by molecular docking and molecular dynamics (MD) simulations. The human body can absorb 33 compounds derived from Curculigo spp. In addition, 58 nodes and 62 edges generated a network analysis with the DM target. The highest degree of the compound–target–disease pathway was for orcinol glucoside, AKR1B1, autoimmune diabetes, bile acid and bile salt metabolism. Furthermore, the computational docking method on Curculigo spp. compounds with the highest degree revealed that orcinol glucoside interacted with PTPN1 through a hydrogen bond and resulted in a binding energy of −7.2 kcal mol−1. Through hydrogen bonds, orcinol glucoside in PTPN1 regulates multiple signaling pathways via the adherens junction pathway, which may play a therapeutic role in DM (type 2 diabetes: obesity). In addition, MD simulation confirmed that orcinol glucoside, is suitable for DM treatment by interacting with PTPN1. Communicated by Ramaswamy H. Sarma