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评价生物素营养的主要技术综述(2)

来源:卫生研究 作者:魏九玲;王竹
发布于:2017-02-22 共6664字
  针对以上方法存在的各种缺陷,2009年日本学者HAYAKAWA等[19]对色谱柱的处理进行改进,利用胰蛋白酶处理的抗生物素蛋白固定色谱柱(Bioptic AV-1,33 mm × 4. 6 mm i. d.) 特异性分离纯化生物素,然后用衍生剂ADAM将其衍生化为荧光 性 的biotin-ADAM酯,再 通 过 激发 波 长365 nm、发射波长412 nm下测定biotin-ADAM酯的荧光度确定生物素含量。结果显示血浆生物素回收实验回收率高达98%,血浆中游离生物素回收率为(70. 7 ± 10. 9)%(CV为15. 4%)。该方法分析速度快、可靠、敏感、准确性高,同时不受其他营养素、抗生物素物质的干扰。
  
  3. 5. 2 GC / MS法1989年MOCK等[20]使用GC / MS法测定成年人尿液中3HIA,同时实验处理过程中引入了3HIA内标,测得尿中3HIA的含量为(112 ± 38)μmol/24 h肌酐。实验发现尿液中有机酸浓度和酰基肉碱底物水平的变化与体内生物素水平有明显的相关性,提示可作为评价生物素 营 养 状 况 的 有 效 指 标。 GC /MS法 测 定3HIA,样品制备过程复杂、耗时长; 技术要求高;同时3HIA的标记物在微量的水中就会水解,要求对样品及时分 析,使 得GC /MS的 推 广 使用受限。
  
  3. 5. 3 UPLC-MS / MS法THOMAS等[21]针对上述缺点进行改进,采用UPLC-MS /MS测定8个健康成 年 人 正 常 尿 样3HIA含 量,其 平 均 值 为(8. 5 ± 3. 2)mmol/mol肌酐。与GC /MS的结果相比后,两 种 方 法 测 定 数 据 之 间 的 相 关 性 为0. 97. BOGUSIEWICZ等[22]使 用 该 方 法 测 定10个生物素缺陷成年人尿液中酰肉碱底物浓度的结果显示: 随着生鸡蛋蛋白摄入时间的延长,尿液中Pc∶ MMc、3HIAc∶ MGc、Ac∶ Mc比值明显上升,分别代表了羧化酶PCC、MCC和ACC活性的下降。研究结果显示这3对比值可以较好地反映人体边缘性生物素缺乏状态。这3对比值中的一项或3项联合使用对于发现孕妇早期生物素缺乏具有重要的意义。UPLC-MS /MS可以精确地分析生物素相关代谢产物的含量,不需要对样品进行提取和衍生化处理[22].尿液中3对肉碱底物比值的测定,不受样品处理时间的影响,同时不需要个体酰基肉毒碱内标或制作标准曲线[21,23-25],检测能力高、花费少,适合大人群快速测定工作。
  
  3. 5. 4 LC-MS / MS法 近年来HORVATH等[23]建立了LC-MS /MS法测定生物素缺陷成年人血浆中3HIA-肉碱的含量,而3HIA-肉碱的生成与生物素代谢途径中MCC活性下降有关[26],而MCC的活性( 排除MCC基因的缺陷) 与体内生物素的水平密切相关。HORVATH等[23]使用该方法测定生物素缺陷者尿液中3HIA-肉碱的浓度,标准曲线回归系数为0. 9992,准确度为3. 79% ~ 5. 8%RE.HORVATH等[24]同时对有无液固萃取或液液萃取过程(SPE) 结果做了比较,结果发现二者之间存在强相关性(r = 0. 996) ,可以将SPE过程省略,提高分析速率。
  
  血浆中3HIA-肉碱较少受到肾功能的影响,使用LC-MS /MS测定3HIA-肉碱,通过测定准确度、精确度、检测限和动态范围来校正多种潜在性可能影响或引起机体生物素缺乏的因素[23].同时LC-MS /MS测定3HIA-肉碱内标误差要比PCC的误差小,在各种液体基质中相对比较稳定,储存条件分布范围: 室温~ - 80 ℃[27].LC-MS /MS法测定 尿 液 中3HIA-肉 碱 的 浓 度 要 比 测 定 血 清3HIA-肉碱更方便,因为尿样的处理相对简单、花费低,没有SPE过程; 兼具血清3HIA-肉碱测定的优点,便于在临床上推广使用[25].
  
  4展望
  
  目前关于生物素营养状况评价方法的研究较多,研究趋势主要集中在以下几个方面: (1) 确定有效的生物标志物,能够反应生物素的代谢及生物作用水平; (2) 相关指标在人体内的正常范围值; (3) 各指标不同生物作用水平之间的关联性;(4) 基质较复杂样品如血浆、尿液中生物素及相关代谢产物含量的测定技术尚不成熟,需要建立敏感、高效和快捷的色谱技术。因此,关于生物素营养状况评价方法还有待深入研究,为生物素代谢评价及生物学应用方面提供依据。
  
  参考文献
  
  [1]KUROISHI T,ENDO Y,MURAMOTO K,et al.Biotin deficiency up-regulates TNF-alpha productionin murine macrophages[J]. J Leukoc Biol,2008,83(4) :912-920.
  [2]PINDOLIA K,JORDAN M,GUO C,et al.Development and characterization of a mouse withprofound biotinidase deficiency:a biotin-responsiveneurocutaneous disorder[J]. Mol Genet Metab,2011,102(2) :161-169.
  [3]ZEMPLENI J,WIJERATNE S S,KUROISHI T.Biotin[M]/ / ERDMAN J W,Jr,MACDONALDI A,ZEISEL S H eds. Present Knowledge in Nutrition,10th edition. ILSI. Wiley-Blackwell,2012.
  [4]HASSAN YI,ZEMPLENI J. A novel,enigmatichistone modification:biotinylation of histones by holo-carboxylase synthetase[J]. Nutr Rev,2008,66:721-725.
  [5]MATHEY K C,GRIFFIN J B,ZEMPLENI J. Biotinsupply affects expression of biotin transporters,biotinylation of carboxylases and metabolism ofinterleukin-2 in Jurkat cells[J]. J Nutr,2002,132(5) :887-892.
  [6]BURKHOLDER P R,MCVEIGH I. Synthesis ofVitamins by Intestinal Bacteria[J]. Proc Natl AcadSci USA,1942,28(7) :285-289.
  [7]MOCK D M,MOCK N I,NELSON R P,et al.Disturbances in biotin metabolism in childrenundergoing long-term anticonvulsant therapy[J]. JPediatr Gastroenterol Nutr,1998,26(3) :245-250.
  [8]ZEMPLENI J,MOCK D M. Marginal biotindeficiency is teratogenic[J]. Proc Soc Exp BiolMed,2000,223(1) :14-21.
  [9]SEALEY W M,STRATTON S L,MOCK D M,etal. Marginal maternal biotin deficiency in CD-1 micereduces fetal mass of biotin-dependent carboxylases[J]. J Nutr,2005,135(5) :973-977.
  [10]MOCK D M,QUIRK J G,MOCK N I. Marginalbiotin deficiency during normal pregnancy[J]. Am JClin Nutr,2002,75(2) :295-299.
  [11]MOCK D M,STADLER D D. Conflicting indicatorsof biotin status from a cross-sectional study of normalpregnancy[J]. J Am Coll Nutr,1997,16(3) :252-257.
  [12]STRATTON S L,BOGUSIEWICZ A,MOCK M M,et al. Lymphocyte propionyl-Co A carboxylase and itsactivation by biotin are sensitive indicators ofmarginal biotin deficiency in humans[J]. Am J ClinNutr,2006,84(2) :384-388.
  [13]BOGUSIEWICZ A,HORVATH T D,STRATTON SL,et al. Measurement of acylcarnitine substrate toproduct ratios specific to biotin-dependentcarboxylases offers a combination of indicators ofbiotin status in humans[J]. J Nutr,2012,142(9) :1621-1625.
  [14]MISHRA S,STORER M B,SHERWIN C M,et al.A simple binding assay for the direct determination ofbiotin in urine.[J]. Clin Chim Acta,2005(12) :60-66.
  [15]ENG W K,GIRAUD D,SCHLEGEL V L,et al.Identification and assessment of markers of biotinstatus in healthy adults[J]. Br J Nutr,2013,110(2) :321-329.
  [16]MOCK D M,MALIK M I. Distribution of biotin inhuman plasma:most of the biotin is not bound toprotein[J]. Am J Clin Nutr,1992,56(2) :427-432.
  [17]MOCK D M,LANKFORD G L,CAZIN J,Jr. Biotinand biotin analogs in human urine:biotin accountsfor only half of the total[J]. J Nutr,1993,123:1844-1851.
  [18]MOCK D M,LANKFORD G L,MOCK N I. Biotinaccounts for only half of the total avidin-bindingsubstances in human serum[J]. J Nutr,1995,125:941-946.
  [19]HAYAKAWA K,KATSUMATA N,ABE K,et al.Wide range of biotin(vitamin H)content infoodstuffs and powdered milks as assessed by high-performance affinity chromatography[J]. Clin PediatrEndocrinol,2009,18(1) :41-49.
  [20]MOCK D M,JACKSON H,LANKFORD G L,MOCK N I. Quantitation of urinary 3-hydroxyisovaleric acid using deuterated 3-hydroxyisovaleric acid as internal standard[J].Biomed Environ Mass Spectrom,18:652-656.
  [21]HORVATH T D,MATTHEWS N I,STRATTON SL,et al. Measurement of 3-hydroxyisovaleric acid inurine from marginally biotin-deficient humans byUPLC-MS / MS[J]. Anal Bioanal Chem,2011,401(9) :2805-2810.
  [22]BOGUSIEWICZ A,HORVATH T D,STRATTON SL,et al. Measurement of acylcarnitine substrate toproduct ratios specific to biotin-dependentcarboxylases offers a combination of indicators ofbiotin status in humans[J]. J Nutr,2012,142(9) :1621-1625.
  [23]HORVATH T D,STRATTON S L,BOGUSIEWICZA,et al. Quantitative measurement of plasma 3-hydroxyisovaleryl carnitine by LC-MS / MS as a novelbiomarker of biotin status in humans[J]. AnalChem,2010,82(10) :4140-4144.
  [24]HORVATH T D,STRATTON S L,BOGUSIEWICZA,et al. Quantitative measurement of urinaryexcretion of 3-hydroxyisovaleryl carnitine by LC-MS /MS as an indicator of biotin status in humans[J].Anal Chem,2010,82(22) :9543-9548.
  [25]MAEDA Y,ITO T,OHMI H,et al. Determinationof 3-hydroxyisovalerylcarnitine and other acylcarnitinelevels using liquid chromatography-tandem massspectrometry in serum and urine of a patient withmultiple carboxylase deficiency[J]. J Chromatogr BAnalyt Technol Biomed Life Sci,2008,870(2) :154-159.
  [26]MOCK D M,MOCK N I,STEWART C W,et al.Marginal biotin deficiency is teratogenic in ICR mice[J]. J Nutr,2003,133(8) :2519-2525.
  [27]ROSCHINGER W,MILLINGTON D S,GAGE D A,et al. 3-Hydroxyisovalerylcarnitine in patients withdeficiency of 3-methylcrotonyl Co A carboxylase[J].Clin Chim Acta,1995,240(1) :35-51.
原文出处:魏九玲,王竹. 生物素营养状况评价方法[J]. 卫生研究,2016,(02):302-305.
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