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Neo Cremar Co., Ltd. · 韩国DNF-10® 低分子酵母肽DNF-10® low-molecular-weight yeast peptide

韩国 Neo Cremar 出品的酵母水解物,肽段分子量小于 10 kDa,美国 FDA GRAS 通知在案。

A yeast hydrolysate from Neo Cremar, Korea: peptides below 10 kDa, with a US FDA GRAS notification on file.

DNF-10 低分子酵母肽

酿酒酵母水解物(含麦芽糊精载体)Saccharomyces cerevisiae hydrolysate with maltodextrin carrier

生物来源 Source
酿酒酵母 Saccharomyces cerevisiae
形态 Form
浅黄至棕色粉末,30–40 目
蛋白 Protein
≥ 40%(批次典型值约 56%)
分子量 MW
肽段平均 ≤ 10 kDa(超滤分级)
载体 Carrier
麦芽糊精约 20%,喷雾干燥
水分 Moisture
≤ 8%
保质期 Shelf life
36 个月,室温避光防潮
法规身份 Status
美国 FDA GRAS 通知;韩国食品原料;中国准入路径以单品资料为准

FDA GRASNon-GMO 声明无溶剂工艺声明韩国 · 欧盟 · 德国专利

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它是什么What it is

DNF-10 是酿酒酵母经蛋白酶水解、固液分离和小分子膜分级后得到的可溶性混合物,以麦芽糊精为载体喷雾干燥成粉。它不是单一纯化肽,而是由游离氨基酸、短肽、糖类和酵母矿物质组成的复合原料,质量以组成分布和指纹图谱定义。

DNF-10 is the soluble fraction of brewer's yeast after enzymatic hydrolysis, solid–liquid separation and low-molecular-weight membrane fractionation, spray-dried on a maltodextrin carrier. It is a defined mixture of free amino acids, short peptides, carbohydrates and yeast minerals rather than a single purified peptide, so quality is specified by composition and fingerprint.

  1. 酵母原料Yeast raw material
  2. 蛋白酶水解Protease hydrolysis
  3. 压滤 / 固液分离Filtration / solid–liquid separation
  4. 超滤,目标 < 10 kDaUltrafiltration, target < 10 kDa
  5. 0.2 μm 微滤 · 蒸发浓缩0.2 μm microfiltration · evaporation
  6. 90 °C 热杀菌Heat sterilisation at 90 °C
  7. 加麦芽糊精 · 喷雾干燥Maltodextrin added · spray drying
  8. 筛分 · 磁选 · 包装Sieving · magnetic separation · packing

组成与规格Composition & specification

FDA GRAS 通知的 4 批分析平均值:游离氨基酸约 38%,3–7 肽约 8%,8–28 肽约 0.8%,未检出 29 肽以上组分;含谷氨酸、天冬氨酸、丙氨酸、赖氨酸、亮氨酸及 GABA。供应商营养成分表:蛋白 59.5 g/100 g、碳水 28.4 g、脂肪 2.9 g、灰分 4.8 g、钾 3.8 g。

Four-batch averages in the FDA GRAS notice: free amino acids about 38%, 3–7-residue peptides about 8%, 8–28-residue peptides about 0.8%, none above 29 residues; glutamic and aspartic acid, alanine, lysine, leucine and GABA are reported. Supplier nutrition data: protein 59.5 g/100 g, carbohydrate 28.4 g, fat 2.9 g, ash 4.8 g, potassium 3.8 g.

研究方向:能量摄入与体重管理Research area: energy intake and weight management

以下为已发表研究的设计与观察结果摘录,供研发与法规评估参考;不构成对原料或终端产品的功能宣称。

Design and reported observations of published studies, provided for R&D and regulatory review only. Not a functional claim for the ingredient or any finished product.

  • 2011

    随机对照,20 名女性,1 g/天,4 周

    Randomised controlled, 20 women, 1 g/day, 4 weeks

    报告组间体重差约 −0.97 kg,BMI 改善;体脂与围度多项未达显著。

    Reported between-group weight difference of about −0.97 kg with BMI improvement; most fat-mass and circumference measures not significant.

  • 2014

    安慰剂对照,54 名完成者,1 g/天,10 周

    Placebo-controlled, 54 completers, 1 g/day, 10 weeks

    报告体重 −2.60 kg 对 +0.83 kg,脂肪量 −2.00 kg 对 +1.12 kg,腰围 −5.04 cm 对 +0.83 cm;后期记录能量摄入下降。

    Reported body weight −2.60 kg vs +0.83 kg, fat mass −2.00 kg vs +1.12 kg, waist −5.04 cm vs +0.83 cm; lower energy intake recorded later in the study.

  • 2017

    对照试验,30 名肥胖女性,0.5 g/天,8 周

    Controlled trial, 30 obese women, 0.5 g/day, 8 weeks

    报告体重 −1.61 kg 对 +0.09 kg,脂肪量 −2.02 kg 对 −0.04 kg,并记录食欲与甜食偏好自评。

    Reported body weight −1.61 kg vs +0.09 kg, fat mass −2.02 kg vs −0.04 kg, with self-rated appetite and sweet-food preference.

  • 2025

    系统综述与 Meta 分析,6 项酵母水解物 RCT,共 262 人

    Systematic review and meta-analysis, 6 yeast-hydrolysate RCTs, 262 participants

    汇总体重平均差约 −3.08 kg,BMI −0.87,脂肪量 −1.93 kg;腰围差异未达显著。作者将证据确定性评为低。

    Pooled mean difference in body weight about −3.08 kg, BMI −0.87, fat mass −1.93 kg; waist not significant. Authors rated certainty of evidence as low.

安全性数据Safety data

人体研究周期 4–10 周,未报告治疗相关严重不良事件。2021 年大鼠试验:急性 5,000 mg/kg 与 90 天 1,000 mg/kg/天未见明显毒性。酵母来源,酵母或酶制剂过敏者、痛风及高尿酸人群、孕哺期与儿童缺乏直接数据,配方设计时应予提示。

Human studies ran 4–10 weeks with no treatment-related serious adverse events reported. A 2021 rat study found no overt toxicity at 5,000 mg/kg acute and 1,000 mg/kg/day for 90 days. As a yeast-derived material, note yeast or enzyme allergy, gout and hyperuricaemia, and the absence of direct data in pregnancy, lactation and children when formulating.

应用Applications

固体饮料、代餐粉、压片糖果、胶囊、功能性饮料。人体研究用量 0.5–1 g/天。模型体系中小分子组分在 140–160 °C、30 分钟条件下较稳定;实际配方仍需做杀菌与货架期验证。

Powdered beverages, meal-replacement powders, pressed tablets, capsules and functional drinks. Doses used in human studies: 0.5–1 g/day. Low-molecular-weight fractions were stable at 140–160 °C for 30 minutes in model systems; sterilisation and shelf-life must still be validated in the final formula.

专利与商标Patents & trademarks

  • KR 10-0999429酵母水解物及其制法韩国,有效至 2030-04
  • KR 10-1372526含酵母水解物的组合物(与高丽大学共有)韩国,有效至 2032-05
  • EP 2564860 B1欧洲专利,德国生效有效至 2031-04
  • DNF-10®Neo Cremar 注册商标韩国、欧盟、美国、中国等

资料Documents

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本页信息来自供应商文件与公开发表的研究,供研发与法规评估参考,不代表原料或终端产品在中国可直接宣称相应功能。

Information on this page comes from supplier documents and published research and is provided for R&D and regulatory review. It does not constitute or permit any health-function claim for the ingredient or finished products sold within China.

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