# Rapid Restoration of Circulating Vitamin B12 Levels by Using Oral Sucrosomial® Vitamin B12 in Metformin-Associated B12 Deficiency: Results from a Double-Blind, Placebo-Controlled Randomized Clinical Trial

**Authors:** Gabriele Conti, Allah W. Kalo, Ikram Ujjan, Aisha Aslam, Amjad Khan, Nazia M. Memon, Shair Z. Kakar, Naseer Ahmed, Shifa Zahid, Germano Tarantino, Elisa Brilli

PMC · DOI: 10.3390/pharmaceutics18020237 · 2026-02-13

## TL;DR

A new oral vitamin B12 supplement rapidly corrects deficiency in diabetes patients taking metformin, who often struggle with absorption issues.

## Contribution

The study demonstrates the efficacy of a lipid-based Sucrosomial® vitamin B12 formulation in correcting B12 deficiency in metformin-treated T2DM patients.

## Key findings

- Sucrosomial® vitamin B12 significantly increased circulating B12 levels faster than placebo in metformin-treated individuals.
- A higher proportion of participants achieved normalized B12 concentrations within three weeks.
- Improvements in biologically active HoloTC levels indicate enhanced B12 availability.

## Abstract

Background/Objectives: Vitamin B12 deficiency is common in individuals with type 2 diabetes mellitus (T2DM) receiving long-term metformin therapy, primarily due to impaired intestinal absorption. Conventional oral B12 supplementation is often associated with delayed or inconsistent biochemical correction. A lipid-based Sucrosomial® delivery system has been shown to improve circulatory vitamin B12 levels in healthy adults with deficiency, and the present study evaluates its performance in the clinically challenging context of metformin-treated individuals with T2DM, a population characterized by pharmacologically impaired intestinal vitamin B12 absorption. Methods: This multicentre, double-blind, placebo-controlled, parallel-group randomized clinical trial evaluated the efficacy, safety, and tolerability of a Sucrosomial® vitamin B12 formulation in adults with T2DM receiving metformin and presenting with vitamin B12 deficiency. Participants were randomized (1:1) to receive oral Sucrosomial® vitamin B12 (1000 µg daily; n = 25) or placebo (n = 25) for three weeks. Serum total vitamin B12 and holotranscobalamin (HoloTC), the biologically active fraction of vitamin B12, were assessed at baseline and during follow-up, with time-to-normalization and safety analyses performed. Results: Sucrosomial® vitamin B12 supplementation resulted in rapid and sustained increases in circulating vitamin B12 levels, with early separation from placebo, and a substantially higher proportion of participants achieved normalization of serum vitamin B12 concentrations within the three-week period. Parallel improvements in HoloTC levels indicated enhanced biologically active vitamin B12 availability, and the intervention was well tolerated with no clinically relevant safety concerns. Conclusions: These findings demonstrate that an oral Sucrosomial® vitamin B12 formulation can achieve rapid and reliable biochemical repletion of both total and biologically active vitamin B12 in metformin-treated adults with T2DM, despite pharmacologically impaired intestinal absorption, while maintaining a favourable safety and tolerability profile.

## Linked entities

- **Chemicals:** metformin (PubChem CID 4091), vitamin B12 (PubChem CID 73415824)
- **Diseases:** type 2 diabetes mellitus (MONDO:0005148), vitamin B12 deficiency (MONDO:0020696)

## Full-text entities

- **Genes:** TCN2 (transcobalamin 2) [NCBI Gene 6948] {aka D22S676, D22S750, II, TC, TC II, TC-2}, CUBN (cubilin) [NCBI Gene 8029] {aka IFCR, IGS, IGS1, MGA1, gp280}, CBLIF (cobalamin binding intrinsic factor) [NCBI Gene 2694] {aka GIF, IF, IFMH, INF, TCN3}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** celiac disease (MESH:D002446), neurological symptoms (MESH:D009461), pernicious anemia (MESH:D000752), B12 Deficiency (MESH:D014806), diabetes (MESH:D003920), injury to (MESH:D014947), gastrointestinal symptoms (MESH:D012817), hepatic dysfunction (MESH:D008107), metabolic disturbances (MESH:D024821), bacterial overgrowth (MESH:D001765), cognitive impairment (MESH:D003072), stage (MESH:D062706), diabetic peripheral neuropathy (MESH:D010523), hypersensitivity (MESH:D004342), megaloblastic anemia (MESH:D000749), T2DM (MESH:D003924), renal disease (MESH:D007674), Crohn's disease (MESH:D003424), diabetic neuropathy (MESH:D003929), gastrointestinal disorders (MESH:D005767), hematological abnormalities (MESH:D006402), intestinal malabsorption (MESH:D008286)
- **Chemicals:** iron (MESH:D007501), tricalcium phosphate (MESH:C018392), B12 (MESH:C034730), phospholipid (MESH:D010743), water (MESH:D014867), Metformin (MESH:D008687), methylmalonic acid (MESH:D008764), magnesium (MESH:D008274), lecithin (MESH:D054709), calcium (MESH:D002118), lipid (MESH:D008055), Vitamin B12 (MESH:D014805), homocysteine (MESH:D006710), vitamin D3 (MESH:D002762), HoloTC (-)
- **Species:** Helianthus annuus (common sunflower, species) [taxon 4232], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944164/full.md

---
Source: https://tomesphere.com/paper/PMC12944164