Bryan Helsey
Department of Biomolecular Science and Translational Medicine, Quezon Medical Center, Quezon, Philippines

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Tinospora crispa Phytosome Enhances Oral Bioavailability and Glycemic Control in Streptozotocin-Induced Diabetic Rats Dedi Sucipto; Taufiq Indera Jayadi; Bryan Helsey
Eureka Herba Indonesia Vol. 7 No. 1 (2026): Eureka Herba Indonesia
Publisher : HM Publisher

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37275/ehi.v7i1.143

Abstract

Diabetes mellitus remains a major global health challenge with rising prevalence in Southeast Asia, where traditional herbal remedies continue to play a significant role in disease management. Tinospora crispa (L.) Hook. f. & Thomson (Menispermaceae), locally known as brotowali in Indonesian jamu medicine, exhibits anti-diabetic properties attributed to its alkaloid and diterpenoid constituents; however, the oral bioavailability of its key bioactive compound berberine remains limited at approximately 5%. This study evaluated the pharmacokinetic enhancement and anti-diabetic efficacy of a novel Tinospora crispa phytosome in streptozotocin (STZ)-induced diabetic rats. Thirty male Wistar rats were allocated to five groups (n = 6): normal control, diabetic control, diabetic plus metformin (200 mg/kg), diabetic plus T. crispa free extract (400 mg/kg), and diabetic plus T. crispa phytosome (400 mg/kg), given orally for 28 days. The phytosome achieved a 3.14-fold enhancement in relative oral bioavailability (AUC0–24: 1524.7 ± 185.4 versus 486.3 ± 62.8 ng·h/mL, p < 0.001) and a higher peak plasma berberine concentration (Cmax: 387.2 ± 42.3 versus 124.5 ± 18.7 ng/mL, p < 0.001). After 28 days, the phytosome group showed significant reductions in fasting blood glucose (148.6 ± 19.2 versus 328.4 ± 42.5 mg/dL, p < 0.001) and HbA1c (6.1 ± 0.6 versus 9.2 ± 1.1%, p < 0.001), with an improved lipid profile comparable to metformin and large effect sizes (Cohen's d: 3.51–6.22). These findings indicate that phytosome technology effectively enhances the bioavailability and anti-diabetic efficacy of T. crispa, supporting its development as a standardized herbal complementary therapy for diabetes mellitus.
Reading the Epigenetic Clock: A Comparative Analysis of DNA Methylation Markers for Age Estimation in Semen, Saliva, and Touch DNA Febria Suryani; Bryan Helsey; Leonardo Simanjuntak; Karina Chandra; Mustafa Mahmud; Lisha Sandrina; Ahmad Erza
Sriwijaya Journal of Forensic and Medicolegal Vol. 3 No. 1 (2025): Sriwijaya Journal of Forensic and Medicolegal
Publisher : Phlox Institute: Indonesian Medical Research Organization

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.59345/sjfm.v3i1.233

Abstract

Introduction: The capacity to predict an individual's age from biological evidence constitutes a significant advancement in forensic intelligence. DNA methylation, a stable epigenetic mark, provides a molecular basis for "epigenetic clocks." However, the operational reliability of these clocks necessitates rigorous validation across diverse biological samples and populations, particularly for challenging, low-template touch DNA evidence. Methods: Following approval from the Ethical Committee of CMHC Indonesia (No. 128/EC/CMHC/2023), we recruited 150 healthy Indonesian male volunteers aged 18-65. Semen, saliva, and high-yield standardized touch DNA samples were collected. DNA was extracted, quantified fluorometrically, and subjected to bisulfite conversion with efficiency controls. The methylation levels of a curated five-CpG panel (ELOVL2, FHL2, TRIM59, KCNQ1DN, C1orf132) were quantified using a rigorously controlled pyrosequencing workflow. Body-fluid-specific age prediction models were developed using multiple linear regression, validated with 10-fold cross-validation, and assessed for statistical assumptions including multicollinearity. Results: The models for semen and saliva demonstrated high predictive accuracy, yielding Mean Absolute Deviation (MAD) values of 3.19 years (R²=0.94) and 3.55 years (R²=0.92), respectively. The model developed from high-yield touch DNA was less precise but still highly informative, with a MAD of 5.49 years (R²=0.85). All models satisfied the assumptions of linear regression, with Variance Inflation Factors below 2.5 indicating low multicollinearity. The 95% prediction intervals were narrowest for semen, reflecting its superior precision. Conclusion: This study validates a robust, targeted epigenetic panel for age prediction in a Southeast Asian population. We present highly accurate, tissue-specific models for semen and saliva, suitable for immediate consideration in forensic casework. The touch DNA model, while requiring cautious interpretation, provides a valuable framework for generating investigative leads from trace evidence. Our findings underscore the critical importance of tissue-specific modeling and provide a detailed methodological and statistical blueprint for the responsible implementation of forensic age estimation.