Source of raw material
Goat meat (chevon) from hind legs of adult male goats (9-11 months old) was procured from local market of Mathura (U.P.). The meat was deboned, trimmed-off separable fat and connective tissue. Approximately four kg meat were kept for conditioning in a refrigerator at 4±1
oC for 6-8 h and then frozen at -18
oC for a period of three months to conduct various trials of the study. The samples were used after partial thawing for 15 h at 4
oC. The study was carried out during the period of April, 2013 to February, 2015, in the Department of Livestock Products Technology, College of Veterinary Science, DUVASU, Mathura, (U.P.).
Spice mix
The ingredients in desired ratio
Anise (10%), black pepper (5%), capsicum (10%), caraway (10%), cardamom (4%), cinnamon (4%), cloves (2%), coriander (15%), cumin (20%), dry ginger (10%) and turmeric (10%) were procured from local market, dried at 45±2
oC for 2 hours followed by grinding and sieving through 100 meshes. The spice mix was stored in low density polyethylene bags and used as per requirement.
Chemicals and other ingredients
All the chemicals used in the study were of analytical grade and procured from Hi Media laboratories (P) Ltd, Mumbai. Ingredients used in the study were procured from standard firm and local market as per availability and requirement of the study. Low density Polyethylene (LDPE) bags of 250 gauge thickness were sourced from local market for packaging and were pre-sterilized by exposing to U.V. light for 30 minutes before use.
Preparation of chevon patties
Lean meat was cut into smaller chunks and minced in a Sirmen mincer (MOD- TC 32 R10 U.P. INOX, Marsango, Italy) with 6 mm plate followed by 4 mm plate. Meat emulsion for patties were prepared in Bowl Chopper [MOD C 15 2.8G 4.0 HP, Marsango, Italy] as per the Formulation (Table 1). Adequate care was taken to keep the end point temperature below 18
oC by preparing the emulsion in cool hours of morning, by addition of meat and other ingredients in chilled/partially thawed form and by addition of crushed ice or ice water. About 50 g of emulsion was moulded on steel plate with circular ring (55X20 mm). Patties were cooked in a pre-heated convection oven at 180
oC for 14 min. after which they were turned and allowed to get cooked for 4 more minutes to get internal temperature about 75
oC. The patties were packed in 0.002 inches thickness of LDPE (low-density polyethylene) pouches and stored at refrigerated temperature (4±1
oC) for further study.
Analytical procedure
Physico-chemical properties
pH
pH was determined by using digital pH meter (WTW, Germany, model pH 330i) by immersing the spear type combination electrode (Sentix®, Germany) directly into minced meat sample.
Prior to measurement, pH meter was calibrated every time as per the manufacturer’s instructions using known buffers of pH 7.0 and 4.01. Reading was taken twice for each sample and average of reading was taken as pH of sample.
Emulsion stability
The emulsion stability was determined by the method of
Baliga and Madaiah (1970) with minor modifications. Twenty five grams of meat emulsion was taken in polyethylene bag and heated in thermostatically controlled water bath at 80
oC for 20 min. after cooling and draining the exudates, the cooked mass was weighed. The percentage of cooked mass was expressed as emulsion stability.
Cooking yield
The weights of chevon patties were recorded before and after cooking. The cooking yield was calculated as under and expressed as percentage
(Murphy et al., 1975).
Proximate analysis
Moisture, protein fat, fiber and ash contents were determined as per
AOAC (1995) method.
Moisture protein ratio
This was calculated by ratio of the moisture and protein content in the sample by using formula for 100 g of samples.
Moisture protein ratio = Moisture% / Protein%
Moisture-retention and fat retention
Moisture retention and Fat retention were determined according to equation by
El-Magoli et al. (1996) and
Murphy et al. (1975) respectively.
Cholesterol content
Total cholesterol was determined as per
Zlatkis et al (1953) with slight modifications. Lipid extract was prepared by mixing one gram of sample with 10 ml of freshly prepared 2:1 Chloroform: Methanol solution and homogenizing it in a blender. Homogenate was filtered using Whatman filter paper No. 42 and 5 ml of filtrate was added with equal quantity of distilled water, mixed and centrifuged at 3000 rpm for 7 min. Top layer (methanol) was removed by suction. Volume of bottom layer (Chloroform) having cholesterol was recorded. The O.D. of standard and sample against blank was taken at 560 nm. Total cholesterol mg per cent was recorded as follows:
Estimation of mineral
The mineral contents were estimated as method described by
Horowitz (1965). The digested samples were analyzed on atomic absorption spectrophotometer (AAS 400 Perkin Elmer, USA) for calcium (Ca), iron (Fe), manganese (Mn) and zinc (Zn) estimation, while sodium (Na) and potassium (K) were estimated by a flame photometer for which the volume was made up to 1000 ml.
Texture profile analysis
Texture profile analysis (TPA) was performed (
Bourne, 1978) using homogeneous sample (1.5 mm X1.5 mm X1.5 mm) for each treatment which was compressed to 10 mm (1 cm) of original height through miniature Ottowa and Kramer shear cell platen probe. Cross head speed of 2.00 mm per second, post test speed 10.00 mm per sec. target mode distance 10.00 mm was used. The following parameters were determined
viz. Hardness (N/cm
2) = maximum force required to compress the sample(H); Adhesiveness (Ns/g sec) = work necessary to pull the compressing plunger away from the sample; Cohesiveness (Ratio) = Extent to which samples could be deformed prior to rupture (A2/A1, A1 being the total energy required for first compression and A2 total energy required for second compression) and Gumminess (N/cm
2 or g/mm
2) = force necessary to disintegrate a semi solid sample for swallowing (HX Cohesiveness).
Instrumental color
Color profile was measured using Lovibond Tintometer (Model: RT-300, UK) set at 2 of cool white light (D65) and known as L*, a* and b* values. L* value denotes (brightness 100) or lightness (0), a* (redness/greenness), b* (yellowness/blueness) values (
Hunter and Harold, 1987).
Sensory evaluation
Panelists were selected from post-graduate students and staff of Veterinary College based on performance in screening test. Four training sessions were held to familiarize the panelists with the developed product characteristics to be evaluated and the scale to be used. Sensory evaluation was carried out in forenoon session (one hour before lunch) by an experienced seven member panel. Panelists were asked to evaluate the samples for general appearance, flavor, texture, saltiness, juiciness, mouth coating and express their overall acceptability using 8-point hedonic scale (
Keeton, 1983), where 8 denoted extremely desirable and 1 denoted extremely undesirable. Samples were internally cooked to 75°C and were served in random order at a temperature of approximately 50°C. At a time total of three samples (one from each treatment) were served to each panelist to compare the products.
Statistical analysis
The data obtained in the study on various parameters were statistically analyzed on ‘SPSS-16.0’ software package as per standard methods of
Snedecor and Cochran (1995). Duplicate samples were drawn for each parameter and the experiment was replicated thrice (n=6). Sensory evaluation was performed by a panel of seven member judges three times, so total observations being 21 (n=21) Data were subjected to one way analysis of variance, homogeneity test and Duncan’s multiple range test (DMRT) for comparing the means to find the effects between samples.