1. Introduction
Dairy products, as an important source of dietary nutrition for humans, have consistently been a research hotspot in food science due to their nutritional value and health benefits. In recent years, with China’s continuous economic development and the steady increase in per capita disposable income, per capita dairy consumption levels have also risen accordingly. As one of the important milk sources in desert and semi-desert regions, camel milk, favored by consumers for its rich nutritional components and good digestibility has gradually gained global attention for its unique nutritional composition and potential health benefits [
1,
2]. Camel milk contains not only abundant protein, unsaturated fatty acids, amino acids, and vitamins, but its mineral element profile also exhibits significant characteristics [
3]. The protein content in camel milk is comparable to that of cow milk, typically ranging from 3.0% to 3.4% [
4]. Its lipid profile is characterized by a high content of long-chain unsaturated fatty acids, particularly polyunsaturated fatty acids (PUFA), which account for a significant proportion of the total fatty acids [
5]. It has been reported that camel milk contains higher levels of cysteine and tryptophan compared to cow milk, while differences are also observed in other amino acids such as lysine [
5]. It is particularly superior to cow milk and goat milk in the content of trace elements such as zinc and iron, while its balance ratio of calcium and magnesium is closer to human physiological needs [
6]. Furthermore, besides its unique nutritional components, the enzymatic hydrolysates of camel milk possess distinct biological functions that can assist in and alleviate various diseases [
7]. Studies indicate that camel milk has healthcare effects including anti-inflammatory and immunomodulatory effects, as well as the ability to alleviate diabetes, liver injury, colitis, and kidney disease [
8,
9,
10], providing a scientific basis for its development as a high-value-added health food.
Although research on the nutritional value of dairy products is relatively comprehensive, systematic horizontal comparison of mineral element composition across different types of milk, such as camel, horse, and cow milk, remains insufficient. Meanwhile, growing consumer demand for personalized nutrition and functional foods is driving the dairy market toward diversification and health-oriented products. In this context, a detailed analysis of the mineral characteristics of camel milk and their correlation with human health could address gaps in fundamental research and offer valuable insights for product development and nutritional applications. This research aims to systematically compare the differences in mineral element content between camel milk and traditional dairy products (cow milk, goat milk, horse milk), as well as the variations in mineral element content of camel milk across different geographical regions. The study employs modern analytical techniques, including inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma optical emission spectrometry (ICP-OES), to characterize these differences. It focuses on revealing the distribution patterns of mineral elements in camel milk and their nutritional significance. The findings will provide a scientific basis for further exploring the functional properties of camel milk and optimizing the structure of dairy product consumption while also offering a theoretical foundation for the sustainable development of camel milk resources and precision nutrition strategies.
2. Materials and Methods
2.1. Experimental Time and Location
Animal experiments were approved by the Animal Welfare and Ethics Committee of Xinjiang Agricultural University (2024018).
The milk samples utilized in this study were collected between 15 and 19 May 2024, from three distinct geographical locations in Xinjiang, China: Yumin County (82°59′ E, 46°12′ N), Tacheng City; Fuhai County (87°30′ E, 47°00′ N), Altay Prefecture; and Huocheng County (80°52′ E, 44°02′ N), Ili Prefecture. These sites are separated by more than 400 km and exhibit diverse topographical and ecological conditions, including variations in soil mineral composition, water sources, and climate, which are known to influence the mineral content of milk from grazing livestock.
2.2. Milk Sample Collection and Preservation
For the current experiment, conducted in Yumin County, Tacheng City, Xinjiang, eight samples of Bactrian camel milk (Camel Milk group), cow milk (Cow Milk group), goat milk (Goat Milk group), and horse milk (Horse Milk group) were collected. All samples were obtained from lactating animals that were grazing without supplementary feed and were within 90–120 days of lactation.
Additionally, eight samples of Bactrian camel milk were collected under the same conditions (grazing without supplementary feed, lactation period 90–120 days) in Fuhai County, Altay Prefecture, and Huocheng County, Ili Prefecture (referred to as Altay and Ili, respectively). After collection, the milk samples were aliquoted into 5 mL sterile cryovials, immediately placed in liquid nitrogen for preservation, transported to the laboratory, and stored at −80 °C for subsequent analysis.
2.3. Measured Indicators and Methods
2.3.1. Instruments and Equipment
The analysis and sample preparation procedures involved in this study required the use of a series of high-precision instruments (
Table 1).
2.3.2. Reagents and Chemicals
Reagents: nitric acid (HNO3), guaranteed reagent (GR) grade, Knowles Reagent; all water used in the experiment was GR grade. Element standards: single-element standard solutions (1000 mg/L) of Ca, P, K, Na, Mg, Zn, Fe, Sr, Cu, Ba, Ni, Mn, Cr, Se, As, Mo, V, Sb, Cd, Be, Co, and Ti, purchased from the National Analysis Center for Nonferrous Metals and Electronic Materials.
2.3.3. Sample Pretreatment
The milk samples were thawed and shaken thoroughly. A 0.5 g aliquot of the milk sample was weighed and placed into a microwave digestion vessel, and 6 mL of nitric acid solution was added. After capping and standing for 1 h, the vessel was placed in the microwave digestion system for gradient digestion (First stage: temperature 120 °C, holding time: 5 min; Second stage: temperature 150 °C, holding time: 5 min; Third stage: temperature 190 °C, holding time: 20 min). After digestion and cooling, the vessel was removed. The inner cap was rinsed with a small amount of water, and the digestion vessel was placed in an ultrasonic water bath for ultrasonic degassing for 5 min. The solution was then diluted to volume with pure water for analysis. A blank test was performed simultaneously.
2.3.4. Preparation of Standard Solutions
Elements Cr, V, Se, Co, Ni, As, Mo, and Sb were detected by inductively coupled plasma mass spectrometry (ICP-MS). Different volumes of element standards were accurately pipetted and diluted to 50 mL with 1% nitric acid to prepare standard curves with six concentration gradients: V, Cr, As, Se, Co, Ni, Be, Cd, Ti: 0, 1.00, 5.00, 10.00, 30.00, 50.00 μg/L; Mo, Sb: 0, 0.100, 0.500, 1.00, 3.00, 5.00 μg/L. Elements Ca, K, Mg, Na, Zn, Fe, Cu, Mn, Sr, and P were detected by inductively coupled plasma optical emission spectrometry (ICP-OES). Similarly, they were diluted to 50 mL with 1% nitric acid to prepare standard curves with six concentration gradients: Sr: 0, 0.0500, 0.200, 0.500, 0.800, 1.00 mg/L; Ca, K, Mg, Na, P: 0, 5.00, 20.0, 50.0, 80.0, 100 mg/L; Fe and Zn: 0, 0.250, 1.00, 2.50, 4.00, 5.00 mg/L; Ba, Mn, and Cu: 0, 0.0250, 0.100, 0.250, 0.400, 0.500 mg/L.
2.3.5. Instrumental Conditions
Inductively coupled plasma mass spectrometry (ICP-MS) operating reference conditions: RF power: 1500 W; Plasma gas flow: 15 L/min; Carrier gas flow: 0.80 L/min; Sampling depth: 8~10 mm; Auxiliary gas flow: 0.40 L/min; Helium gas flow: 4~5 mL/min; Nebulizer chamber temperature: 2 °C; Points per peak: 1~3; Sample uptake rate: 0.3 r/s; Replicates: 2~3.
Inductively coupled plasma optical emission spectrometry (ICP-OES) operating reference conditions: Power: 1150 W; Plasma gas flow: 15 L/min; Auxiliary gas flow: 0.5 L/min; Nebulizer gas flow: 0.65 L/min; Analysis pump speed: 50 r/min.
2.3.6. Data Processing
Experimental data were collated using Microsoft Office 2019 (Microsoft, Redmond, WA, USA). Results are expressed as mean standard deviation. Differences between samples were analyzed using SPSS Statistics Software Version 27.0 (IBM, New York, NY, USA) through one-way analysis of variance (ANOVA) and Duncan’s multiple range test. Statistical significance was set at p < 0.05, and extreme significance was set at p < 0.01. The images in the text were created using OriginLab Origin 2024 (Version 2024, OriginLab Corporation, Northampton, MA, USA). Factor analysis, principal component analysis (PCA), and linear discriminant analysis (LDA) were employed to explore the underlying structure and patterns within the mineral content data. PCA was used to reduce dimensionality and visualize natural groupings among samples based on mineral composition, while LDA was applied to maximize separation among pre-defined milk type groups and identify the most discriminant minerals. Factor analysis aided in interpreting latent variables influencing mineral profiles.
4. Discussion
Due to variations in genetics, environment, and digestive/absorption mechanisms among different species, the mineral content in milk is significantly influenced by the species. This research found that camel milk is rich in macro elements. The contents of Ca, P, and K were the highest in the camel milk, followed by Na and Mg. The contents of Ca and P in camel milk were very significantly higher than in cow milk and horse milk, and the contents of K and Na were very significantly higher than in horse milk. Studies indicate that the contents of Ca, P, and K in camel milk are higher than in cow milk [
11]. The high concentration of electrolytes like sodium and potassium in camel milk is closely related to the extremely arid environment of its habitat [
12]. Camels transfer high osmotic pressure minerals through their milk to maintain the fluid balance of their calves under water-scarce conditions [
13]. Genomics studies have shown that the strong expression of the AQP1 gene in renal tubular epithelial cells in camels enhances water reabsorption capacity, while the upregulation of Na
+/K
+ -ATPase activity in milk may be achieved through epigenetic regulation, ensuring efficient mineral transport into the milk [
14]. The enrichment of electrolyte-related mineral elements in camel milk reflects the species’ metabolic adaptation to the desert niche [
15]. If the body’s K is high and Na is low, leading to a decrease in blood Na/K, it can cause an increase in blood pressure. The results of this research show that the Na/K ratio in camel milk is significantly higher than in goat milk and horse milk, indicating that camel milk is relatively friendly for patients with blood pressure elevation-related diseases. The Ca and P contents in camel milk were very significantly higher than in cow milk and horse milk. According to research data [
16,
17], the calcium content in camel milk is 154.57–186.87 mg/100 g. In comparison, the calcium content in cow milk is 112–134 mg/100 g, while that in horse milk is lower, at only 60–80 mg/100 g for liquid milk. The calcium content in mature camel milk is approximately 30–40% higher than in cow milk and more than twice as high as in horse milk. The phosphorus content in cow milk is 59–121 mg/100 g, while in horse milk it is 40–60 mg/100 g. The phosphorus content in camel milk is approximately 20–50% higher than in cow milk and about twice as high as in horse milk. Camels live in arid and high-temperature environments, and their milk needs to provide minerals required for rapid skeletal development in calves. The high calcium and phosphorus content in the milk may be an evolutionary adaptive trait.
Camel milk provides abundant trace elements. The study by Chen L et al. [
18] showed that the contents of Zn, Ni, Se, Cu, Cr, and As in camel milk are higher than those in cow milk. We found that, among the trace elements in camel milk, the content of Zn is relatively high, followed by Fe and Sr, while the contents of Ni, Se, Cu, Cr, As, Be, Co, Cd, V, Sb, and Ti were significantly higher than those in other types of milk; the contents of Zn and Fe were higher than those in cow milk. Trace elements not only reflect the nutritional value of milk [
19], but also play certain roles in promoting immune function, energy metabolism [
20,
21], enhancing metabolic processes, and reducing oxidative stress damage in organisms [
22,
23]. Moreover, they help protect young camels from the influences of arid environments. The high levels of Fe and Cu in camel milk are associated with hemoglobin metabolism and adaptation to oxidative stress in camels, which can enhance the survival ability of calves in hypoxic environments [
18]. Zn and Se are crucial for immunity and antioxidation, and camels transmit these elements through their milk to strengthen the resistance of their offspring in harsh environments [
24]. The significant loadings of Se, Sb, and Cd in Principal Component 1 (46.259%) suggest that these elements may have a common source or bioaccumulation characteristics [
25,
26]. The high loadings of Ca, Mg, and P in Principal Component 2 (19.642%) reflect the biological role of macro mineral elements; their content differences may be directly related to mammary gland biosynthesis capacity [
27], species metabolic characteristics, and dietary nutritional levels [
28]. The cluster analysis results visually presented the differential distribution of milk samples based on species, confirming that mineral fingerprints can serve as effective biomarkers for milk source identification. Chen Lu et al. [
18] made similar observations that milk samples were divided into different clusters based on PCA scatter plots.
Among the five macro mineral elements, only the K content in Tacheng camel milk was significantly higher than in Altay camel milk. The Na/K ratio in Tacheng camel milk was 0.37, significantly lower than in Altay (0.43) and Ili (0.52). This electrolyte balance characteristic may enhance the heat stress tolerance. Regarding trace elements, the Tacheng region’s camel milk exhibited highly significant increases in 11 trace mineral elements (including Zn, Be, and V) compared to camel milk from the other two regions. The Sr content in Ili region camel milk was very significantly lower than in the other two regions. These differences may generally be related to climate, soil, and feed. Concerning trace metal elements like Pb, Cd, and Zn, concentrations in Tacheng were generally 1 to 3 times higher than in Ili and Altay. Liu, Y. et al. [
29] found that the enrichment of trace elements such as Cu, Cd, Zn, and Pb in the northern Xinjiang region is dominated by human activities. Backward trajectory cluster analysis indicated that trace elements in the Tacheng region are more influenced by air mass transport from Kazakhstan. The high content of Ni, Mn, Cr, Co, and Ti in the Tacheng region may be related to the weathering of mafic rocks in this area, as these rocks are typically rich in iron-group elements [
30]. The Altay region has a temperate continental cold climate, strongly influenced by Siberian cold air, with relatively high soil organic matter content but lower soil development due to the cold climate [
31]. The Ili region has a temperate semi-humid climate, significantly influenced by the westerlies and topographic uplift, with soils mainly consisting of sierozem soils, and locally, chestnut soil and meadow soil [
32]. The Tacheng region has a temperate semi-arid climate, combining continental and mountainous characteristics, also dominated by sierozem.
5. Conclusions
This study quantified 22 mineral elements in Bactrian camel milk collected from Tacheng, Altay, and Ili, as well as in cow, goat, and horse milk from the Tacheng region. The results demonstrate that camel milk exhibits significantly elevated concentrations of macro elements (Ca, P, K, Na) and certain trace elements (Se, Sr, Ni) compared to other milk types. Multivariate statistical analyses confirmed the discriminative capacity of mineral compositions for milk species identification and revealed a distinct mineral profile in camel milk. Notably, camel milk from Tacheng displayed higher levels of Sr, Ni, and Cr, indicating influences from geo-environmental factors. Linear discriminant analysis (LDA) models were developed for both milk species classification and geographic origin traceability, demonstrating high accuracy for authentication purposes.
These findings provide a scientific basis for the dairy industry to differentiate and valorize specialty milk products, offer guidance for consumer nutritional education, and support the authentication of geographical origin. However, this study did not consider potential changes in mineral levels during the lactation period. Thus, future research should extend the sampling to cover broader geographical regions and longer timeframes to enhance the generalizability and commercial applicability of the model.