MEAT SCIENCE Meat Science 67 (2004) 395–401 www.elsevier.com/locate/meatsci The effects of irradiation on quality of injected fresh pork loins Kathy J. Davis a, Joseph G. Sebranek b,c,*, Elisabeth Huff-Lonergan b, Dong U. Ahn b, Steven M. Lonergan b a Burke Marketing Corp., 1516 South D Ave., Nevada, IA 50201, USA Department of Animal Science, 215 Meat Laboratory, Iowa State University, Kildee Hall, Ames, IA 50011 USA Department of Food Science and Human Nutrition, 215 Meat Laboratory, Iowa State University, Kildee Hall, Ames, IA 50011, USA b c Received 16 June 2003; received in revised form 10 November 2003; accepted 10 November 2003 Abstract A comparison of irradiation effects on injected and uninjected fresh pork loin quality was conducted. Sixty pork loins from pigs of similar genetics were obtained from a pork harvesting facility immediately prior to processing. Thirty loins were injected with a brine composed of 2.17% salt/3.04% phosphate/20.8% lactate brine while thirty were not injected. Injected loins were pumped to 13% added weight. Ten loins of each group of thirty were not irradiated while an additional 10 loins were irradiated at 2.2 kGy and the final ten loins were irradiated at 4.4 kGy. Lipid oxidation, color, purge, volatiles, and tenderness were measured on sections of the treated loins after 0, 7, 21, and 35 days of refrigerated storage. Lipid oxidation was minimal for the 0 and the 2.2 kGy-treated loins, but was significantly greater (P < 0:05) at day 35 for the loins treated with 4.4 kGy. Warner–Bratzler shear (WBS) force measurements were significantly lower (P < 0:05) for the injected loins, but irradiation did not have an effect on shear force. Purge was significantly lower for the uninjected loins irradiated at 2.2 kGy than for those irradiated at 0 and 4.4 kGy. The injection treatment did not alter the effects of irradiation on the quality characteristics measured. Ó 2003 Elsevier Ltd. All rights reserved. Keywords: Irradiation; Injected pork; Tenderness; Lipid oxidation 1. Introduction Safety and quality are of utmost importance to the meat industry. Treatments that have potential to ensure safe, consistent, high-quality products have been a major priority for recent research. Use of ingredients and processing technology such as irradiation appear to have excellent potential, particularly in combination, to achieve both safety and quality improvements. Among the popular products in the meat case today are injected or Ômoisture-enhancedÕ pork. Several ingredients are injected in a brine formulation to improve the consistency and quality of pork and other meat products. The ingredients most commonly included are salt, polyphosphates and lactate. * Corresponding author. Tel.: +1-515-294-1091; fax: +1-515-2945066. E-mail address: sebranek@iastate.edu (J.G. Sebranek). 0309-1740/$ - see front matter Ó 2003 Elsevier Ltd. All rights reserved. doi:10.1016/j.meatsci.2003.11.011 Salt added to the whole muscle meat products is known to increase water retention by increasing myofibrillar spacing. The chloride ion increases electrostatic repulsion between filaments which allows for more water to be absorbed and retained in the filament lattice (Offer & Trinick, 1983). Phosphates work synergistically with salt and allow meat processors to achieve equivalent water-holding capacity with reduced amounts of salt (Offer & Trinick, 1983). Sheard, Nute, Richardson, Perry, and Taylor (1998) found that polyphosphates improved water-holding, tenderness, and juiciness in pork loins. Furthermore, phosphates allow cooking pork to a higher temperature to ensure food safety while still maintaining desirable texture and flavor. While salt and phosphate have been shown to improve tenderness and water-holding capacity in meat, lactate has been included in many formulations as a bacteriostatic agent. Sodium lactate added at 3% lowered aerobic plate counts in comparison to controls at 42 and 84 days in beef top rounds (Papadopoulos, 396 K.J. Davis et al. / Meat Science 67 (2004) 395–401 Miller, Ringer, & Cross, 1991). Increasing sodium lactate in beef top rounds also increased cooking yields (Papadopoulos et al., 1991). Despite the advantages of added ingredients in injected fresh products, the injection process has potential to contaminate the interior of the product with bacteria and this could pose a threat to food safety. Irradiation has been studied extensively for improving the safety of meat products. The USDA approved irradiation of fresh red meats with up to 4.5 kGy and the irradiation of frozen red meats with up to 7.0 kGy (USDA, 1999). Irradiation is not approved currently for processed pork, but it could provide a solution for the potential problem of contamination from injection. Irradiation of meat is a viable way to eliminate foodborne illnesses caused by organisms such as Escherichia coli O157:H7, Salmonellae, Listeria monocytogenes, and Staphylococcus aureus (Dempster, 1985). Most spoilage and pathogenic bacteria, yeasts, and molds can be significantly reduced in number by irradiation at doses between 0.5 and 3 kGy (Dempster, 1985; Murano, 1995). Despite the advantages of irradiation for microbial control, questions have been raised about potential changes in meat quality attributes following irradiation processing. Irradiation of pork has, for example, been reported to result in the production of undesirable volatiles that have been suggested to be the result of oxidation reactions. Ahn, Jo, and Olson (1999) found that these volatiles were not related to lipid oxidation but were caused independently by radiation of protein and lipid molecules. Ahn, Jo, Du, Olson, and Nam (2000) reported that refrigerated storage of irradiated pork patties allowed for dissipation of irradiation-induced volatiles, which were not detected after one week. They also found that pork patties that were irradiated and stored in a vacuum package did not result in increased lipid oxidation. The color of pork can also be affected by irradiation. Nanke, Sebranek, and Olson (1998) found that irradiation induced a bright oxymyoglobin-like pigment in pork chops. The redness increased with increased dose levels. Lightness values were not affected but the yellowness was also increased with doses from 0 to 4.5 kGy and remained constant at higher dosages. If irradiation could be used to reduce the risk of contamination in injected pork products, there are still questions about quality problems that could result from the irradiation treatment. Because phosphates function as antioxidants and chelators in processed meat (Mielche & Bertelsen, 1994), addition of phosphates may reduce quality changes induced in pork by irradiation. Thus, the hypothesis for this study was that injection of fresh pork with phosphate and added water would reduce quality changes observed for irradiation processing of fresh pork cuts. 2. Materials and methods Sixty pork loins were acquired from a commercial facility and were processed 7 days after harvest. Thirty loins were injected (I) with a Townsend Model 1450 injector (Townsend Eng., Des Moines, IA) to 13% final added weight with a brine composed of 3.04% sodium tripolyphosphate, 2.17% sodium chloride, and 20.8% potassium lactate. Following injection, loins were tumbled for 1 h. The remaining 30 loins were not injected (N) or tumbled. Ten loins from each group were cut into four sections and vacuum packaged to serve as unirradiated (0) controls (N, 0 and I, 0). The remaining 40 loins were each cut into four sections and individually vacuum packaged. The loin sections were vacuum packaged with a Multivac Model A6800 vacuum packaging machine (Multivac Inc. Kansas City, MO) in pouches with a O2 transmission rate of 3–6 cc/m2 /24 h at 1 atm, 4.4 °C, and 0% RH, and a water vapor transmission rate of 0.5–0.6 g/645 cm2 /24 h at 100% RH. Packages were stored at 0–2 °C. Immediately after vacuum packaging, 40 loins were transferred to the Iowa State University Meat Laboratory Linear Accelerator Facility (LAF) for irradiation treatments. The facility has a CIRCE IIIR electron beam irradiator (Thomsen CSF Linac., Saint Aubin, France) with an energy level of 10 MeV and a power level of 10 kW. The loins were irradiated with two passes, one on each side. Average dose rate was 92.7 kGy/min and the conveyor speed was 26 m/min for the first side and 12.9 m/min on the second side. The group of 20 loins [10 injected (I, 2.2) and 10 uninjected (N, 2.2)] irradiated at a target dose of 1.5 kGy received an average delivered dose of 2.21 kGy with a maximum dose of 2.91 kGy. The second group of 20 loins [10 injected (I, 4.4) and 10 uninjected (N, 4.4)] loins were irradiated at a target dose of 3.0 kGy and received an average delivered dose of 4.42 kGy with a maximum dose of 5.84 kGy. The doses were confirmed using 99% pure alanine dosimeters (Bruker Inst. Inc., Billerica, MA) placed on cut ends between loin sections. The dosimeters were verified by a EMS 104 Electron Paramagnetic Resonance instrument (Bruker Analytisctie Messtechnik, Karlsruhe, Germany). Samples were collected for analysis immediately following irradiation. Loins were stored at 0–2 °C for 1, 7, 21 or 35 days following the treatment. 2.1. Purge Purge in the packages was measured on day 7, 21, and 35 after processing. To get the initial weight, the vacuum-packaged loin sections were weighed. The loin sample was then removed from the bag, the bag was drained, and an absorbent towel was used to remove excess moisture. The bag and sample were then K.J. Davis et al. / Meat Science 67 (2004) 395–401 reweighed. The purge loss was calculated as the percentage of the loin weight that was lost by removal of moisture. 2.2. Shear force After injection and irradiation, 2.5 cm chops for Warner–Bratzler shear (WBS) force measurement were cut from loins of each treatment, packaged and frozen immediately at )20 °C, or aged for 21 days before freezing at )20 °C. Twenty-two days after freezing, the chops were thawed at 0–2 °C, broiled to an internal temperature of 71 °C and chilled 5–8 h in at 0–2 °C. For the WBS measurement, three cores, each 1 cm in diameter, were cut parallel to the muscle fibers from each chop. The WBS force was measured on each core using a TA.XT2 Texture Analyzer (Texture Technologies Corp., Scarsdale, NY), and the mean shear force calculated for each chop. The tests were performed using Warner–Bratzler Probe and Guillotine Set number TA7B USDA. The probe was programmed to be lowered 30 mm after detection of resistance. The penetration speed was 3.3 mm/s with a post-test speed of 10 mm/s and a pre-test speed of 2.0 mm/s. The WBS measurements for the second set of chops (frozen after aging) were then performed 25 days after freezing in the same manner described above. 2.3. Color measurements Chops (2.5 cm) were cut from the loin sections, allowed to bloom for 10 min at room temperature and measured on the Hunterlab Labscan colorimeter (Hunter Associated Laboratories Inc., Reston, VA). Illuminate A, 10° standard observer, and a 1.3 cm viewing port area were used to measure the Hunter CIE L* (lightness), a* (redness), and b* (yellowness). Three measurements were made on the face of each chop. Color was measured on all 60 samples immediately after injection and irradiation, and repeated on day 7, 21, and 35 of storage. 2.4. Lipid oxidation The day after injection and irradiation were completed, 2-thiobarbituric acid (TBA) measurements (Tarladgis, Watts, Younathan, & Dugan, 1960) were performed on the 60 loin samples to measure lipid oxidation. The TBA measurement was repeated at 7, 21, and 35 days of storage on samples of all 60 loins. 2.5. Volatiles Gas chromatography for detection of volatiles was performed on five of the samples from each treatment group on day 1, 7, 21, and 35, as described by Ahn 397 et al. (1999). Four compounds (methanethiol, methylthio ethane, dimethyl disulfide and hexanal) were selected for monitoring differences between treatments because these four have been reported to be increased by irradiation and/or lipid oxidation (Ahn, Nam, Du, & Jo, 2001). A purge-and-trap apparatus connected to a gas chromatography/mass spectrometry was used to analyze the volatiles that might be responsible for offodors. Precept II and Purge-and-Trap Concentrator 3000 (Tekmar–Dohrmann, Cincinnati, OH) were used to purge and trap volatiles from the loin samples. A gas chromatography (GC) unit (Model 6890, Hewlett– Packard Co., Wilmington, DE) equipped with a mass selective detector (MSD, HP 5973, Hewlett–Packard Co.) was used to characterize and quantify the volatiles observed. For volatiles measurement, a minced meat sample (3 g) was transferred to a 40-ml sample vial, and the headspace was flushed with helium gas (99.999% purity) for 5 s to minimize oxidative changes during holding. A multiple ramped oven temperature program was used. The oven was held at 0 °C for 2.5 min followed by three different ramp temperatures: 2.5 °C/min to reach 10 °C, 5 °C/min until 45 °C was reached, and 10 °C/min to reach a final temperature of 210 °C. Liquid nitrogen was used to cool the oven below ambient temperature. Helium was the carrier gas at a constant pressure of 20.5 psi. Identification of volatiles was achieved by comparing mass spectral data of peak areas of samples with those of the Wiley library (Hewlett–Packard Co.). Selected standards were used to verify the identities of some volatiles. Each peak area was integrated using the Chemstation software (Hewlett–Packard Co.) and reported as the amount of volatiles released (total ion counts 104 ). 2.6. Statistical analysis The statistical analysis was performed with the Statistical Analysis System (SAS, 2000) mixed model procedure. The main effects were irradiation dosage and injection treatment with each compared within each sampling day. Least squares means were used to determine significance at a P < 0:05 level. 3. Results and discussion The overall least squares means for purge loss are reported in Table 1. Injected loins showed significantly less purge than uninjected loins for all irradiation treatment groups. Purge from injected loins was unaffected by irradiation treatment. There was less purge loss in uninjected loins at 7 and 21 days in those samples irradiated at 2.2 kGy (N, 2.2) than either unirradiated samples or those irradiated at 4.4 kGy. Purge was also 398 K.J. Davis et al. / Meat Science 67 (2004) 395–401 Table 1 Purge loss from injected (I) and uninjected (N) fresh pork loins after irradiation Irradiation/Injection treatment N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM Storage time (days) 7 21 a 35 b 2.99 0.33c 1.42b 0.56c 3.05a 0.34c 0.51 4.17a 0.85b 3.26a 0.96b 4.54a 0.96b 0.62 2.63 0.64c 1.89b 0.69c 3.64a 0.48c 0.41 Means within the same column with different superscripts (a–d) are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. less at 35 days for the uninjected, 2.2 kGy treatment but relatively large variation resulted in no statistical significance at 35 days. Lambert, Smith, and Dodds (1992) reported that irradiation of vacuum-packaged fresh pork resulted in decreased purge after 3 days of storage compared to unirradiated product, but increased purge at 14 and 28 days of storage. On the other hand, Luchsinger et al. (1997) reported that irradiation dosage did not affect purge loss. Because there was not a linear relationship between irradiation dose and purge in our study, the practical effects, if any, of irradiation on purge are not clear. The overall least squares means for the WBS force values are shown in Table 2. Injected samples were significantly (P < 0:05) lower in WBS values than uninjected samples. This agrees with previous research on injection and would be expected for the injection treatment (Offer & Trinick, 1983; Sheard et al., 1998). There did not appear to be significant differences (P > 0:05) between irradiation treatments, indicating that irradiation did not have any effect on tenderness. This coincides with the finding of Heath, Owens, and Table 2 Shear (WBS) values (kg/cm2 ) for injected (I) and uninjected (N) fresh pork loins after irradiation Irradiation/Injection treatment N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM Storage time (days) 1 21 a 3.11 2.21b 2.96a 1.79b 2.83ab 1.96b 0.24 2.71a 1.63b 3.10a 1.75b 2.64a 1.71b 0.19 Means within the same column with different superscripts (a–b) are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2 and 4.4 kGy denote the dosage of irradiation the product received in kGy. Tesch (1990) and Niemand, van der Linde, and Holzapeel (1981) who reported that irradiation did not affect tenderness. Our results also demonstrated that the injection process did not alter the effects of irradiation on these products. The main effects of irradiation on color are shown in Table 3. The L* (lightness) values were not significantly different (P > 0:05) between treatments on day 0 or day 7. However, at day 21, uninjected samples were lighter than all the injected treatments. At day 35, uninjected samples all resulted in greater L* values than injected samples, but the differences were not significant. Table 3 also compares the a* values between treatments. Generally, the 4.4 kGy dosage resulted in a higher a* value for both the injected and uninjected chops. This is in agreement with Nanke et al. (1998) who reported that irradiation increased redness in pork. The b* values found in Table 3 were not consistently different (P < 0:05) over time. Lipid oxidation, as determined by TBA measurements, is shown in Table 4. Within injection treatments, the TBA values increased with irradiation dosage at all sampling times (1, 7, 21, 35 days). This can be interpreted as increased lipid oxidation resulting from irradiation treatment. However, no TBA values observed were greater than 0.24 which means that relatively little lipid oxidation occurred. Luchsinger et al. (1997), also reported an increase in TBA values as irradiation dose was increased for aerobically packaged ground beef patties, but observed a decrease for samples in vacuum packages. Results from the volatiles analysis using gas chromatography measurements are shown as selected compounds in Tables 5–7. Methanethiol, methylthio ethane, dimethyl disulfide, and hexanal were chosen to compare the treatments because the first three have been reported to be increased by irradiation, causing an unappetizing odor (Ahn et al., 2000; Ahn et al., 2001; Schweigert & Doty, 1954). Hexanal was included because it is a volatile produced from lipid oxidation (Ahn et al., 2001) and one that may also increase with irradiation. Irradiation treatments resulted in production of methanethiol (Table 5) while none of this volatile compound was observed for unirradiated treatments. In general, the higher irradiation doses (N, 2.2; N, 4.4; I, 4.4) also resulted in significantly greater amounts of (P < 0:05) of methanethiol than low-dose treatments (N, 0; I, 0) and (I, 2.2), suggesting greater production of this volatile compound as irradiation dosage was increased. Table 5 also shows that the methanethiol levels declined over time in treatments N, 2.2, N, 4.4, and I, 4.4, suggesting that this volatile dissipated. The methanethiol appears to be reduced by the injection treatment but this is significant for only three of the eight irradiation treatment/time combinations. However, the times K.J. Davis et al. / Meat Science 67 (2004) 395–401 399 Table 3 Color (L*, a*, b*) values for injected (I) and uninjected (N) fresh pork loins after irradiation Injection/Irradiation treatment Color value Storage time (days) 0 7 a 21 a 35 a N, 0 kGy L* a* b* 54.64 5.72d 16.98w 56.19 4.18ef 16.73w 57.64 3.38e 16.10w 59.59a 4.23de 18.30w I, 0 kGy L* a* b* 57.23a 4.26de 16.58w 53.53a 3.08f 15.81w 54.71b 2.74de 15.67xy 55.62a 2.84f 16.56wx N, 2.2 kGy L* a* b* 56.12a 3.97e 15.11y 56.25a 5.28de 16.80w 58.20a 4.23de 15.78w 59.88a 4.50de 18.06w I, 2.2 kGy L* a* b* 54.94a 4.12de 15.41xy 54.59a 4.28ef 15.48w 54.40b 3.98de 15.28wx 57.39a 3.41ef 16.04x N, 4.4 kGy L* a* b* 55.93a 5.77d 15.46xy 56.78a 6.28d 16.63w 59.39a 5.43d 16.29w 60.37a 5.48d 17.78wx I, 4.4 kGy L* a* b* 56.20a 5.50d 15.98wx 53.55a 6.13d 15.84w 54.82b 5.57d 14.75xy 55.10a 5.34d 16.67wx SEM SEM SEM L* a* b* 1.58 0.59 0.50 1.54 0.42 0.51 1.39 0.59 0.44 1.88 0.69 0.56 Means within the same column for L* (a–c), a* (d–f), and b* (w–z) with different superscripts are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. Table 4 TBA values (mg malonaldehyde/kg meat) for injected (I) and uninjected (N) fresh pork loins after irradiation Injection/ Irradiation treatment N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM Storage time (days) 1 0.08bcd 0.07d 0.11abc 0.08bcd 0.13a 0.10abc 0.01 7 0.10bc 0.08d 0.13ab 0.10bc 0.14a 0.12ab 0.01 21 0.10c 0.07d 0.12b 0.11bc 0.12b 0.15a 0.02 35 0.09cd 0.08d 0.10c 0.10c 0.19b 0.24a 0.02 Table 5 Methanethiol (ion count 1000) production from injected (I) and uninjected (N) fresh pork loins after irradiation Injection/Irradiation treatment Storage time (days) 0 7 21 35 N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM 0d 0d 2908.8b 151.4c 7575.0a 5206.8ab 910.9 0d 0d 358.0c 0d 7302.2a 4131.6b 440.1 0c 0c 1139.8b 123.6b 4738.0a 3759.6a 746.2 0c 0c 1195.4ab 558.6ab 2777.8a 1897.0a 1053.1 Means within the same column with different superscripts (a–d) are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. Means within the same column with different superscripts (a–d) are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. when differences are significant are all either at day 0 or day 7 which may indicate that differences were reduced over time by dissipation. Also, the I, 2.2 kGy treatment resulted in values within one standard deviation of zero, suggesting that volatiles the values were not different than zero and were suppressed by the injection treatment. Similar results were observed for dimethyl disulfide (Table 6) except that a low level of this volatile was observed in samples that were not irradiated. Methylthio ethane (Table 7) was present only in the irradiated samples but did not dissipate during storage. Hexanal (data not shown) increased slowly during storage but no significant effects of irradiation or injection treatments were observed. Hexanal is a volatile often used to indicate lipid oxidation (Ang & Lyon, 1990), but does not always correlate directly the TBA analysis. In this study, the TBA values (Table 4) indicated significant effects of irradiation treatments. However, all the TBA values were relatively low (<0.24) meaning that very little oxidation occurred. 400 K.J. Davis et al. / Meat Science 67 (2004) 395–401 Table 6 Dimethyl disulfide (ion count 1000) production from injected (I) and uninjected (N) fresh pork loins after irradiation Injection/ Irradiation treatment Storage time (days) 0 7 N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM 73.2d 32.4d 3158b 1415.2c 6583.6a 5270.6a 783.1 50.6c 56.8c 460.8b 284.6b 5197a 5597a 614.7 21 132.2cd 53.8cd 2194.2b 460.2c 4810.2a 4499.4a 755.7 35 0c 59.7c 2861a 655.0bc 2010.4a 1257.4ab 932.7 Means within the same column with different superscripts (a–d) are significantly different (P < 0:05). N, uninjected; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. Table 7 Methythioethane (ion count 1000) production from injected (I) and uninjected (N) fresh pork loins after irradiation Injection/ Irradiation treatment Storage time (days) 0 7 21 35 N, 0 kGy I, 0 kGy N, 2.2 kGy I, 2.2 kGy N, 4.4 kGy I, 4.4 kGy SEM 0c 0c 98.2ab 65.0b 128.0a 122.0a 29.8 0c 0c 86.6ab 58.4b 155.2a 138.8a 24.2 0c 0c 128.4ab 62.6b 155.2a 157.8a 21.2 0c 0c 164.0ab 101.2b 222.0a 205.8a 28.9 Means within the same column with different superscripts (a–c) are significantly different (P < 0:05). N, uninjected product; I, injected. 0, 2.2, and 4.4 kGy denote the dosage of irradiation the product received in kGy. 4. Conclusions The results of this experiment indicated that injection of pork loins with a salt/phosphate/lactate brine had relatively little effect on quality changes often observed for irradiation. Some of the volatiles increased by irradiation appeared to be reduced by the injection treatment especially during the first 7 days following irradiation, but this effect was not consistent for all treatment/storage time combinations studied. Lipid oxidation, as measured by TBA values, increased with irradiation dosage, but the change in TBA value with irradiation did not seem to be affected by injection treatment. Likewise, color changes were observed with irradiation treatment but injection did not appear to have an influence on irradiation-induced color changes. In uninjected loins, purge seemed to be decreased at 2.2 kGy, but not at 4.4 kGy and further investigation of irradiation effects on purge is required. Injection treatment resulted in decreased WBS force values indicating a consistent tenderness improvement regardless of the irradiation treatment. Thus, injection of fresh pork with a salt/phosphate/lactate brine did not change tenderness or color characteristics of irradiated pork loins. At the same time, injection processing may have potential to decrease production of some volatiles produced by irradiation. The role of specific ingredients for control of volatiles produced during irradiation of pork cuts requires further investigation. Acknowledgements This journal paper of the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa, Project Nos. 3700 and 3705, was supported by Hatch Act and State of Iowa funds. A portion of this project was funded by the National Pork Board on behalf of the Iowa Pork Producers Association. The authors express gratitude to Mike Holtzbauer, Marcia King-Brink and Randy Petersohn for technical assistance. References Ahn, D., Jo, C., Du, M., Olson, D., & Nam, K. (2000). Quality characteristics of pork patties irradiated and stored in different packaging and storage conditions. 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