| Literature DB >> 35277018 |
Rahul Mehra1, Renu Garhwal1, Karnam Sangwan1, Raquel P F Guiné2, Edite Teixeira Lemos2, Harpal Singh Buttar3, Pradeep Kumar Singh Visen4, Naveen Kumar1, Anuradha Bhardwaj5, Harish Kumar1.
Abstract
Bovine colostrum (BC) is the initial mammary secretion after parturition, which is nature's bountiful source consisting of nutritional and bioactive components present in a highly concentrated low-volume format. All mammalian newborns require colostrum to enhance physiological processes such as lifelong immunity, gastrointestinal development, and resistance to microbial infections. The genetic, environmental, and processing methods can all have an impact on the biochemical contents of BC and its supplements. BC and its derivatives have been intensively researched for their potential use in functional foods, medicines, and animal feed. Evidence from clinical studies suggests that BC products are well-tolerated, nontoxic, and safe for human ingestion. Functional foods, feed, and pharmaceutical formulations based on bovine colostrum are playing noteworthy roles in the development of innovative products for promoting health and the prevention of chronic illnesses. This systematic review sheds light on recent research on (a) the effects of processing techniques on BC components, (b) emerging techniques used in the isolation and identification of novel components, (c) BC-based functional foods for human consumption and animal feed supplements, and (d) the role of BC in current drug delivery, as well as future recommendations.Entities:
Keywords: bovine colostrum; food and feed supplements; nutritional and bioactive components; prophylaxis
Mesh:
Year: 2022 PMID: 35277018 PMCID: PMC8840100 DOI: 10.3390/nu14030659
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 5.717
Difference in immunoglobulin concentration between human and bovine colostrum.
| Immunoglobins | |||
|---|---|---|---|
| Bovine (mg/mL) | Milk | Colostrum | Serum |
| IgG1 | 0.59 | 20–200 | 14.0 |
| IgG2 | 0.12 | 12.0 | 11.0 |
| IgM | 0.05 | 4.20 | 3.1 |
| IgA | 0.14 | 3.90 | 0.4 |
|
| |||
| Total IgG | 0.04 | 0.43 | 12.1 |
| IgM | 0.10 | 1.59 | 0.9 |
| IgA | 1.00 | 17.35 | 2.5 |
Data adapted from [14,15,17].
Figure 1Overview of bovine colostrum nutritional and bioactive components with their medicinal and industrial applications.
Modern techniques employed in the isolation and identification of BC components.
| Technique/Component | Study Aim | Subject/Sample | Key Findings | Reference |
|---|---|---|---|---|
| Isobaric tags for relative and absolute quantitation (iTRAQ)-coupled LC-MS | Proteomic analysis of whey protein in BC, mature milk, and human milk. | Colostrum (0–5 days) collected from Chinese Holsten ( | iTRAQ-coupled LC-MS is the most advanced, reliable, and precise technique in the proteomic quantification of milk from different origins and lactation. | [ |
| Laser-perturbation 2-D correlation Raman spectroscopy | Exploration of laser perturbation 2-D correlation Raman spectroscopy method for the reliable and rapid assessment of the quality of BC-based products. | Colostrum samples in milligrams were loaded in porous chips, followed by the Raman spectral analysis. The excitation wavelength was 785 nm and laser power was 450 nm. | The intended approach is simple, rapid (<5 min), and inexpensive.$$$The correlation coefficient analysis assists in improving the difference in experimental samples and improved spectral resolution.$$$In the future, this approach might be utilized to effectively differentiate milk powder in BC-based products. | [ |
| UHPLC-QTOF-MS | Characterize and compare the lipids in mature milk and BC based on ultra-high-performance liquid chromatography–quadrupole time of flight mass spectroscopy (UHPLC-QTOF-MS) lipidomics. | Mature milk and BC. | A total of 335 lipids belonging to 13 subclasses were identified in both mature milk and BC.$$$ | [ |
| Split trehalase immunoglobulin G assay (STIGA) | Develop a novel method for the estimation of IgG in BC and serum at the farm level. | BC ( | STIGA is a single step assay that requires less time as compared to other methods which directly measure IgG and could be a promising method to use for the detection of IgG at the farm level. | [ |
| Dye affinity chromatography | Purification of lactoperoxidase (LPO) from whey by employing dye affinity chromatography. | Triazine dye ( | Dye–Sepharose ( | [ |
| Mixed-mode chromatography | Develop an efficient, cost-effective procedure to isolate pure IgG from colostrum whey with minimal activity loss. | Two modes were used to separate the IgG from colostrum whey. Capto multimodal chromatography material (MNC) and MEP HyperCel matrix were used to capture IgG. | The authors isolated pure IgG (130–150 g) from 3 L of whey in five hours. This mixed-mode chromatography results in the purity of 96.1% IgG. This technique can be used in the future for the pure, stable, and active isolation of IgG from bovine milk and colostrum. | [ |
| Transmission infrared (IR) spectroscopy and Brix refractometer | Determine the effectiveness of transmission infrared spectroscopy (IR) and Brix refractometer (optical and digital) in the estimation of colostrum IgG concentration. | Colostrum samples of Holstein cow ( | Transmission infrared (IR) spectroscopy is an accurate and rapid method to determine the colostrum quality, i.e., IgG, in lab-based testing where the Brix refractometer (digital and digital) is less effective. Moreover, the study suggests that transmission infrared spectroscopy is effective at the lab scale, while the Brix (digital and digital) can be used to determine the colostrum quality at the farm level. | [ |
| Exosomal microRNAs | Identify and compare the exosomal $$$microRNAs in both milk and colostrum. | Dogu Anadolu Kirmizisi and Holstein cows, | A total of 795 miRNAs were expressed and identified differently, out of which 545 were identified as miRNAs, of which 250 were identified as novel miRNAs. These miRNAs regulate milk protein and fat metabolism. | [ |
| Neutral and acidic oligosaccharides | Isolation of neutral and acidic oligosaccharides from BC and goat milk for infant formula. | 20 mL of BC (0–3 days) after parturition, human milk ( | The oligosaccharides from goat milk have more potential in terms of adherence inhibition and safety to be utilized in infant formula. | [ |
| N-glycoproteomes | Characterize and compare whey N-glycoproteomes from BC, HC, and mature milk. | A bioinformatics analysis using liquid chromatography (LC)–tandem mass spectrometry. Colostrum and mature milk were collected from Holstein cows ( | N-Glycoproteomes were different in BC, HC, and mature milk. N-Glycoproteomes (68, 58, and 98) were identified in all milk samples. The composition of N-glycoproteomes is significantly changed with lactation. | [ |