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At our 17 testing locations in Garland, Maine, Accredited Drug Testing offers a full suite of drug and alcohol screening services. We cater to DOT and non-DOT requirements, providing tests like urine and breath alcohol tests, EtG, and hair drug analysis for personal, work-related, and legal purposes. Offering quick testing results in Garland, ME, our services include SAMSA lab analysis, with most centers just minutes away from your Garland location. We also offer Occupational Health, Clinical Testing, and Background Checks.
Contact us at (800) 221-4291 or register online to schedule a test. Choose your preferred test and location with ease—available for you, your employees, or another party. Booking a test is swift and straightforward; our team is ready by phone or online 24/7. Our efficient process ensures arranging drug testing near Garland is a breeze.
* 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 Garland 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.
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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 recent reports, Penobscot County, where Garland is located, has seen a 15% increase in opioid-related overdoses over the last year.
Garland, nestled in Penobscot County, recorded a 12% rise in admissions for substance abuse treatment programs in 2022.
According to the Penobscot County Sheriff's Office, drug-related arrests in Garland spiked by 20% in the first quarter of 2023.
Emergency services in Penobscot County, covering Garland, responded to 50 drug overdose calls in the past year.
A survey in Garland, within Penobscot County, found that 8% of high school students admitted to using illicit drugs in the last month.
Data indicates that 65% of drug abuse treatment seekers in Garland, Penobscot County, were primarily addicted to opioids.
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 Garland, ME, are increasingly implementing drug testing policies to combat workplace drug issues. These policies align with guidelines from the U.S. Department of Labor, aiming to ensure a drug-free work environment.
Many employers collaborate with local testing facilities to conduct pre-employment screenings and random drug tests. This approach helps maintain safety and productivity while addressing potential substance abuse among employees.
In conjunction with state recommendations, employers in Garland have instituted educational programs focusing on the risks of drug abuse, providing resources for employees who seek help. These initiatives are part of a broader commitment to community wellness and workforce stability.
The government of Garland, ME, located in Penobscot County, collaborates with the Maine Department of Health and Human Services to address drug abuse issues. Initiatives include increased funding for rehabilitation centers and public awareness campaigns.
Further efforts include the support of the Penobscot County Sheriff's Office in increasing patrols and undertaking community outreach programs. These measures aim to curb the spike in drug-related incidents in Garland.
Recent local drug busts in Garland, ME, highlight ongoing law enforcement efforts in tackling drug abuse. The Penobscot County Sheriff's Office conducted a major operation in 2023, resulting in multiple arrests and the seizure of illicit substances.
Community events, such as drug take-back days, have been organized to safely dispose of unused medications, reducing the risk of misuse. These events are part of a larger strategy to engage the community in combatting the local drug problem.
The collaboration between local authorities and federal agencies has been pivotal in disrupting drug trafficking channels. Public engagement and tip lines have significantly contributed to these successes, fostering a community-focused approach to safety.
Accredited Drug Testing offers fast, reliable employment screening services in Garland, ME. Trusted by employers nationwide for accurate results and exceptional service.
Maine Office of Substance Abuse
Penquis
Maine Attorney General's Office
Northern Light Health - Addiction Resource Center
Maine Alliance for Addiction Recovery
Maine Public Health Association
Maine Health Insurance Addiction Resources
211 Maine
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Time was running out before my Cdl got downgraded because of a violation I had on clearinghouse. I couldn't find an employer to send me for my return to duty test, but these guys had my test scheduled and done in the same day! They saved my cdl. Thank you again!
Michael Williams - 12/2/2024
I always have a good experience setting up company driver drug screens through ADT. I'm really happy I found them while searching online, they have made my job much easier.
Exodus Heath - 2/13/2025
I use their service for new hire and DOT employee's. Spoke with Taisha Walker this morning, and she was very helpful. She made the process smooth and seamless.
Christina Galdos - 3/9/2025