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In the New Lancaster, Kansas region, Accredited Drug Testing facilitates all-encompassing drug and alcohol assessments at 40 centers. We cater to both DOT and non-DOT needs, offering urine and breath alcohol tests, EtG alcohol assessments, and hair drug evaluations suitable for individuals, employers, and legal uses. Our New Lancaster centers provide rapid results and SAMSA-approved lab analyses, with same-day options available. Most centers are conveniently located close to residences or workplaces. Additional offerings include Occupational Health, Clinical Testing, and Background Verifications.
To schedule, dial (800) 221-4291 or register through our website. After selecting a test, pick a nearby center for personal, employee, or third-party testing. Booking is quick and straightforward—contact our scheduling team or arrange online any time. Our efficient, user-friendly system ensures drug testing near New Lancaster is simple.
* You must register by phone or online to receive your donor pass/registration prior to proceeding to the testing center. You must bring a valid government issued ID along with the registration/barcode number which was sent to you by email.
When you're searching for drug testing near me or drug testing locations, we provide a simple and convenient process to find a drug and alcohol testing location near you that is certified to provide all of your drug and alcohol testing needs.
At our New Lancaster drug testing collection sites, Accredited Drug Testing provides one of the widest selections of drug and alcohol testing services available. Whether you're an employer, attorney, court, or private individual, we offer both DOT and non-DOT testing options—ranging from rapid tests to comprehensive lab-based screenings—capable of detecting nearly any substance.
DOT Drug Testing and Requirements
DOT Employer Drug Policy Development
If you're an employer needing to test 25 or more employees and looking to save time and money, we offer mobile on-site drug testing where we come to you. Call us today for more information.
In 2020, Johnson County, where New Lancaster is located, reported a 15% increase in opioid-related overdoses.
Methamphetamine was involved in 42% of drug arrests in Johnson County in 2021.
In 2022, Johnson County health services provided addiction treatment to 1,200 residents.
The New Lancaster community health survey 2022 indicated that 8% of teens had used illicit drugs.
Alcohol abuse accounted for 55% of admissions in treatment centers in Johnson County in 2023.
Johnson County law enforcement seized 250 pounds of illegal substances in New Lancaster in 2021.
Drug elimination is the sum of the processes of removing an administered drug from the body. In the pharmacokinetic ADME scheme (absorption, distribution, metabolism, and excretion), it is frequently considered to encompass both metabolism and excretion. Hydrophobic drugs, to be excreted, must undergo metabolic modification making them more polar. Hydrophilic drugs, on the other hand, can undergo excretion directly, without the need for metabolic changes to their molecular structures.
Although many sites of metabolism and excretion exist, the chief organ of metabolism is the liver, while the organ primarily tasked with excretion is the kidney. Any significant dysfunction in either organ can result in the accumulation of the drug or its metabolites in toxic concentrations.
A variety of other factors impact elimination — intrinsic drug properties, such as polarity, size, or pKa. Also other factors include genetic variation among individuals, disease states affecting other organs, and pathways involved in the way the drug distributes through the body, such as first-pass metabolism.
Drug elimination is the removal of an administered drug from the body. It is accomplished in two ways, either by excretion of an unmetabolized drug in its intact form or by metabolic biotransformation followed by excretion. While excretion is primarily carried out by the kidneys, other organ systems are involved as well. Similarly, the liver is the primary site of biotransformation, yet extrahepatic metabolism takes place in a variety of organ systems affecting multiple drugs.
Given the multiple organ systems and the variety of metabolic transformations present, drug elimination can entail a significant degree of complexity. Hydrophilic drugs are typically directly excreted by the kidneys, while hydrophobic drugs undergo biotransformation before excretion. The purpose here is twofold – biotransformation serves both detoxify the exogenous substances as well as to increase their hydrophilicity, ensuring their elimination via the kidneys.
Two broad metabolic pathways of hepatic drug transformation exist. Phase I is the direct modification of the target molecule, whereas phase II entails conjugation of the target to a polar molecule of low molecular weight. Phase I prepare the drug to enter phase II, but single-phase metabolism also exists.
Phase I involves oxidation, reduction, and hydrolysis of the exogenous molecule. These reactions are accomplished by hepatic microsomal enzymes, which reside in the smooth endoplasmic reticulum of the hepatocytes. Best known among them is the cytochrome P450 system, whose enzymes are predominantly involved in oxidative metabolism. Within the cytochrome P450 family (CYP), the enzyme responsible for the metabolism of more than 50% of existing drugs is the CYP3A4. Its activity encompasses various classes of medications, including opioids, immunosuppressants, antihistamines, and benzodiazepines. The enzymes can also be induced or inhibited by a variety of substances they interact with, including pharmaceuticals. The increase in metabolic activity with CYP induction results in a diminished activity of drugs targeted by that particular isoform. Conversely, CYP inhibition will result in increased drug plasma concentration, potentially leading toxicity. The CYP3A4 is induced by phenytoin, phenobarbital, and St. John's wort, while diltiazem, erythromycin, and grapefruit inhibit it. Caution is, therefore, necessary when administering CYP3A4-metabolized drugs in the presence of any of the inhibitors or inducers.
Phase II consists of covalent bonding of polar groups to nonpolar molecules to render them water-soluble and allow renal or biliary excretion. Target molecules enter phase II directly or via initial processing through phase I. A variety of polar adjuncts is transferred, including amino acids, glucuronic acid, glutathione, acetate, and sulfate. Glucuronidation is one of the major pathways of phase II biotransformation. The UDP-glucuronosyltransferase (UGT) enzyme family performs this activity. Typically, glucuronide derivatives possess less or no activity of the original drug, but in some cases, pharmacologically active compounds result. Morphine-6-glucuronide is a phase II metabolite of morphine with significant analgesic activity. As with the CYP enzymes, inducers, and inhibitors of phase II, enzymes exist and may influence the efficacy of drugs that rely on conjugation before excretion.
The first-pass effect is a feature of hepatic metabolism that also plays a role in the elimination of multiple drugs. Here, the enteric consumed drugs are exposed directly to the liver via the portal vein, where they undergo biotransformation before entering the systemic circulation. This activity reduces the bioavailability and needs to be factored into the dose administered to the patient. Intravenously administered drugs are not subject to the first-pass effect.
Extrahepatic drug metabolism takes place in the GI tract, kidneys, lungs, plasma, and skin.
Renal excretion completes the process of elimination that begins in the liver. Polar drugs or their metabolites get filtered in the kidneys and typically do not undergo reabsorption. They subsequently get excreted in the urine. Urinary pH has a significant impact on excretion, as drug ionization changes depending on the alkaline or acidic environment. Increased excretion occurs with weakly acidic drugs in basic urine and weakly basic drugs in acidic urine.
Excretion in the bile is another significant form of drug elimination. The liver can actively secrete ionized drugs with a molecular weight greater than 300 g/mol into bile, from where they reach the digestive tract and are either eliminated in feces or reabsorbed as part of the enterohepatic cycle.
Other pathways of excretion include the lungs, breast milk, sweat, saliva, and tears
Employers in New Lancaster, KS, are taking firm steps against drug abuse by implementing comprehensive drug testing policies. Many businesses use pre-employment screening, random drug tests, and post-accident testing to ensure a drug-free workplace. This not only improves safety but also enhances productivity.
Local companies often rely on resources provided by entities such as the Department of Labor to craft these policies. They are encouraged to use guidelines from the state to balance employee rights with workplace safety. Moreover, periodic workshops are held to educate both employers and employees on the importance of maintaining a drug-free environment.
The Kansas State Government collaborates closely with Johnson County Mental Health department to battle drug abuse in New Lancaster. This partnership focuses on providing resources and treatment facilities for addicts, as well as educational programs aimed at prevention. By enhancing community outreach initiatives, the government aims to reduce the incidence of substance abuse.
Furthermore, the Kansas Bureau of Investigation has also been involved, working with federal bodies like the DEA to track and reduce the flow of illegal drugs into New Lancaster. Joint efforts include increased patrols and investigations that focus on large-scale drug operations. These initiatives have put a significant strain on drug networks within Johnson County.
Recent drug busts in New Lancaster, KS, have underscored the ongoing challenges in the fight against illegal drug distribution. In early 2023, a coordinated operation led to the seizure of significant quantities of methamphetamine, highlighting persistent issues in Johnson County.
The local police department, in collaboration with federal agencies, executed warrants that resulted in multiple arrests. These efforts demonstrated the importance of continued vigilance and cross-agency cooperation in combating drug networks. Such operations are crucial in reducing the availability of illicit drugs on the streets of New Lancaster.
Accredited Drug Testing offers fast, reliable employment screening services in New Lancaster, KS. Trusted by employers nationwide for accurate results and exceptional service.
Kansas Department for Aging and Disability Services
Johnson County Mental Health Department
DCCCA
Kansas Substance Abuse Prevention Coalition
Kansas Family Guidance Center
Central Kansas Foundation
Comcare
Kansas o-drug Help
12 Keys Kansas Drug Rehab
Sunflower Wellness Retreat
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Quickly find a local DOT drug testing center in New Lancaster, KS — fast, reliable, convenient nationwide service!
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Trish last week and Tatiana this week, very fun and easy folks to deal with. Well be using them more and more in the future.
Tom O - 12/19/2024
Trish was amazing and got me through the sytem very fast and swift. I had a hard time hearing her a couple of times, but she was super sweet and helpful throughout the process. Highly recommend her!
Sophia Schutze - 6/19/2024
I've had to use this service twice for out of state physicians we've hired and both times it was super easy. Both customer service reps I spoke with were super helpful and courteous. I won't hesitate to use their service again if needed.
Alicia Rau - 6/19/2024